ENST00000349841.10:c.1562T>A
MANE Select
|
ENSP00000326240.4:p.Val521Asp
|
|
ENST00000349841.9:c.1562T>A
|
ENSP00000326240.4:p.Val521Asp
|
|
ENST00000356716.8:c.1562T>A
|
ENSP00000349150.3:p.Val521Asp
|
|
ENST00000544106.5:c.1483+1140T>A
|
ENSP00000440637.1:n.1483+1140T>A
|
|
ENST00000602751.5:c.*1170T>A
|
ENSP00000473654.1:n.*1170T>A
|
|
NM_001185118.1:c.1562T>A
|
NP_001172047.1:p.Val521Asp
|
|
NM_001185119.1:c.1483+1140T>A
|
NP_001172048.1:n.1483+1140T>A
|
|
NM_018657.4:c.1562T>A
|
NP_061127.1:p.Val521Asp
|
|
NR_033702.1:n.1861T>A
|
|
|
NR_033703.1:n.1875T>A
|
|
|
XM_005247621.3:c.1478T>A
|
XP_005247678.1:p.Val493Asp
|
|
XM_005247622.3:c.1316T>A
|
XP_005247679.1:p.Val439Asp
|
|
XM_005247624.3:c.1220T>A
|
XP_005247681.1:p.Val407Asp
|
|
XM_011512987.1:c.1562T>A
|
XP_011511289.1:p.Val521Asp
|
|
XM_011512988.1:c.1562T>A
|
XP_011511290.1:p.Val521Asp
|
|
XM_005247621.5:c.1478T>A
|
XP_005247678.1:p.Val493Asp
|
|
XM_005247622.4:c.1316T>A
|
XP_005247679.1:p.Val439Asp
|
|
XM_005247624.4:c.1220T>A
|
XP_005247681.1:p.Val407Asp
|
|
XM_017006864.2:c.1562T>A
|
XP_016862353.1:p.Val521Asp
|
|
XM_017006865.2:c.1136T>A
|
XP_016862354.1:p.Val379Asp
|
|
XM_017006866.2:c.1136T>A
|
XP_016862355.1:p.Val379Asp
|
|
XM_017006867.2:c.743T>A
|
XP_016862356.1:p.Val248Asp
|
|
XM_017006868.2:c.659T>A
|
XP_016862357.1:p.Val220Asp
|
|
XR_002959552.1:n.3394T>A
|
|
|
NM_001185118.2:c.1562T>A
|
NP_001172047.1:p.Val521Asp
|
|
NM_018657.5:c.1562T>A
MANE Select
|
NP_061127.1:p.Val521Asp
|
|
NR_033702.2:n.1530T>A
|
|
|
NR_033703.2:n.1544T>A
|
|
|