ID: 131377 | kelch like family member 40 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (42685537..42692544) | KBTBD5, NEM8, SRYP, SYRP | 615340 |
ID: 4633 | myosin light chain 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110910845..110921449, complement) | CMH10, MFM12, MLC-2, MLC-2s/v, MLC-2v, MLC2 | 160781 |
ID: 4654 | myogenic differentiation 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17719571..17722136) | CMYP17, MYF3, MYOD, MYODRIF, PUM, bHLHc1 | 159970 |
ID: 5224 | phosphoglycerate mutase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44062727..44065567, complement) | GSD10, PGAM-M, PGAMM | 612931 |
ID: 29765 | tropomodulin 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151169987..151175981, complement) | SK-TMOD | 605834 |
ID: 1158 | creatine kinase, M-type [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (45306413..45322875, complement) | CKMM, CPK-M, M-CK | 123310 |
ID: 5913 | receptor associated protein of the synapse [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (47437764..47449136, complement) | CMS11, CMS4C, FADS, FADS2, RAPSYN, RNF205 | 601592 |
ID: 7138 | troponin T1, slow skeletal type [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55132698..55149206, complement) | ANM, NEM5, STNT, TNT, TNTS | 191041 |
ID: 6345 | sarcalumenin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4189374..4242080, complement) | SAR | 604992 |
ID: 136371 | ankyrin repeat and SOCS box containing 10 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (151175698..151187792, complement) | GLC1F | 615054 |
ID: 4656 | myogenin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (203083129..203086012, complement) | MYF4, bHLHc3, myf-4 | 159980 |
ID: 146862 | unc-45 myosin chaperone B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (35147817..35189345) | CMYA4, CTRCT43, MFM11, SMUNC45, UNC-45B, UNC45 | 611220 |
ID: 8557 | titin-cap [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39665349..39666554) | CMD1N, CMH25, LGMD2G, LGMDR7, T-cap, TELE, telethonin | 604488 |
ID: 116729 | protein phosphatase 1 regulatory subunit 27 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81833492..81835050, complement) | DYSFIP1 | |
ID: 786 | calcium voltage-gated channel auxiliary subunit gamma 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (67044554..67056797) | CACNLG | 114209 |
ID: 126306 | junctional sarcoplasmic reticulum protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2252252..2256417, complement) | JP-45, JP45 | 608743 |
ID: 200539 | ankyrin repeat domain 23 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (96837912..96844021, complement) | DARP, MARP3 | 610736 |
ID: 186 | angiotensin II receptor type 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (116170744..116174974) | AT2, ATGR2, MRX88 | 300034 |
ID: 779 | calcium voltage-gated channel subunit alpha1 S [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201039512..201112426, complement) | CACNL1A3, CCHL1A3, CMYP18, Cav1.1, DHPRM, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP | 114208 |
ID: 4625 | myosin heavy chain 7 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (23412740..23435660, complement) | CMD1S, CMH1, CMYP7A, CMYP7B, MPD1, MYHCB, SPMD, SPMM | 160760 |