ENST00000356592.8:c.1266G>A
|
|
|
ENST00000361925.9:c.1361G>A
|
ENSP00000354651.5:p.Cys454Tyr
|
|
ENST00000523372.2:c.1324G>A
|
|
|
ENST00000638253.1:n.519G>A
|
|
|
ENST00000638552.1:c.956G>A
|
ENSP00000491763.1:p.Cys319Tyr
|
|
ENST00000638660.1:c.980G>A
|
ENSP00000492869.1:p.Cys327Tyr
|
|
ENST00000638772.1:c.*3862G>A
|
ENSP00000491557.1:n.*3862G>A
|
|
ENST00000638877.1:c.1142G>A
|
|
|
ENST00000639046.1:c.632G>A
|
ENSP00000492659.1:p.Cys211Tyr
|
|
ENST00000639111.2:c.1241G>A
|
ENSP00000492125.2:p.Cys414Tyr
|
|
ENST00000639213.2:c.1265G>A
MANE Select
|
ENSP00000491909.2:p.Cys422Tyr
|
|
ENST00000639278.1:c.1928G>A
|
ENSP00000491958.1:n.1928G>A
|
|
ENST00000639384.1:c.*1446G>A
|
ENSP00000491240.1:n.*1446G>A
|
|
ENST00000639424.1:c.*465G>A
|
ENSP00000491245.1:n.*465G>A
|
|
ENST00000639683.1:c.1199G>A
|
ENSP00000492581.1:p.Cys400Tyr
|
|
ENST00000639975.1:c.1175G>A
|
ENSP00000492096.1:p.Cys392Tyr
|
|
ENST00000640500.1:n.539G>A
|
|
|
ENST00000640739.1:n.6212G>A
|
|
|
ENST00000640910.1:c.703G>A
|
|
|
ENST00000640985.1:c.1178G>A
|
ENSP00000492293.1:p.Cys393Tyr
|
|
ENST00000641017.1:c.1334G>A
|
ENSP00000493461.1:p.Cys445Tyr
|
|
ENST00000356592.7:c.1265G>A
|
ENSP00000349000.3:p.Cys422Tyr
|
|
ENST00000361925.8:c.1241G>A
|
ENSP00000354651.4:p.Cys414Tyr
|
|
ENST00000414552.6:c.1385G>A
|
ENSP00000410732.2:p.Cys462Tyr
|
|
ENST00000522990.5:c.*843G>A
|
ENSP00000430732.1:n.*843G>A
|
|
ENST00000523372.1:c.1362G>A
|
ENSP00000430124.1:n.1362G>A
|
|
NM_000816.3:c.1241G>A
|
NP_000807.2:p.Cys414Tyr
|
|
NM_198903.2:c.1385G>A
|
NP_944493.2:p.Cys462Tyr
|
|
NM_198904.2:c.1265G>A
|
NP_944494.1:p.Cys422Tyr
|
|
NM_001375339.1:c.1256G>A
|
NP_001362268.1:p.Cys419Tyr
|
|
NM_001375340.1:c.*99G>A
|
NP_001362269.1:n.*99G>A
|
|
NM_001375341.1:c.1262G>A
|
NP_001362270.1:p.Cys421Tyr
|
|
NM_001375342.1:c.1238G>A
|
NP_001362271.1:p.Cys413Tyr
|
|
NM_001375343.1:c.1361G>A
|
NP_001362272.1:p.Cys454Tyr
|
|
NM_001375344.1:c.1304G>A
|
NP_001362273.1:p.Cys435Tyr
|
|
NM_001375345.1:c.1175G>A
|
NP_001362274.1:p.Cys392Tyr
|
|
NM_001375346.1:c.1199G>A
|
NP_001362275.1:p.Cys400Tyr
|
|
NM_001375347.1:c.1178G>A
|
NP_001362276.1:p.Cys393Tyr
|
|
NM_001375348.1:c.821G>A
|
NP_001362277.1:p.Cys274Tyr
|
|
NM_001375349.1:c.956G>A
|
NP_001362278.1:p.Cys319Tyr
|
|
NM_001375350.1:c.845G>A
|
NP_001362279.1:p.Cys282Tyr
|
|
NM_198904.3:c.1265G>A
|
NP_944494.1:p.Cys422Tyr
|
|
NM_198904.4:c.1265G>A
MANE Select
|
NP_944494.1:p.Cys422Tyr
|
|