ID: 57126 | CD177 molecule [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (43353686..43366081) | HNA-2a, HNA2A, NB1, NB1 GP, PRV-1, PRV1 | 162860 |
ID: 10544 | protein C receptor [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (35171096..35216259) | CCCA, CCD41, EPCR | 600646 |
ID: 7056 | thrombomodulin [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (23045633..23049672, complement) | AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM, TM | 188040 |
ID: 5657 | proteinase 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (840999..848175) | ACPA, AGP7, C-ANCA, CANCA, MBN, MBT, NP-4, NP4, P29, PR-3, PR3 | 177020 |
ID: 5627 | protein S [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (93873051..93973896, complement) | PROS, PS21, PS22, PS23, PS24, PS25, PSA, THPH5, THPH6 | 176880 |
ID: 5624 | protein C, inactivator of coagulation factors Va and VIIIa [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (127418427..127429242) | APC, PC1, THPH3, THPH4, PROC | 612283 |
ID: 5270 | serpin family E member 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (223975045..224039286, complement) | GDN, GDNPF, PI-7, PI7, PN-1, PN1, PNI | 177010 |
ID: 5197 | platelet factor 4 variant 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73853296..73854483) | CXCL4L1, CXCL4V1, PF4-ALT, PF4A, SCYB4V1 | 173461 |
ID: 5196 | platelet factor 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (73980811..73982124, complement) | CXCL4, PF-4, SCYB4 | 173460 |
ID: 5104 | serpin family A member 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94581426..94593118) | PAI-3, PAI3, PCI, PCI-B, PLANH3, PROCI | 601841 |
ID: 3053 | serpin family D member 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20774113..20787720) | D22S673, HC2, HCF2, HCII, HLS2, LS2, THPH10 | 142360 |
ID: 2266 | fibrinogen gamma chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154604136..154612656, complement) | | 134850 |
ID: 2244 | fibrinogen beta chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154562980..154572807) | HEL-S-78p | 134830 |
ID: 2243 | fibrinogen alpha chain [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (154583126..154590742, complement) | Fib2 | 134820 |
ID: 2165 | coagulation factor XIII B chain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (197038741..197067260, complement) | FXIIIB | 134580 |
ID: 2162 | coagulation factor XIII A chain [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (6144084..6320662, complement) | F13A | 134570 |
ID: 2159 | coagulation factor X [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113122799..113149529) | FX, FXA | 613872 |
ID: 2157 | coagulation factor VIII [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154835792..155022723, complement) | AHF, DXS1253EB, F8C, FVIII, HEMA, THPH13, F8 | 300841 |
ID: 2153 | coagulation factor V [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (169511951..169586481, complement) | FVL, PCCF, RPRGL1, THPH2 | 612309 |
ID: 2149 | coagulation factor II thrombin receptor [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (76716126..76735770) | CF2R, HTR, PAR-1, PAR1, TR | 187930 |