ENST00000349841.10:c.1564C>G
MANE Select
|
ENSP00000326240.4:p.His522Asp
|
|
ENST00000349841.9:c.1564C>G
|
ENSP00000326240.4:p.His522Asp
|
|
ENST00000356716.8:c.1564C>G
|
ENSP00000349150.3:p.His522Asp
|
|
ENST00000544106.5:c.1483+1142C>G
|
ENSP00000440637.1:n.1483+1142C>G
|
|
ENST00000602751.5:c.*1172C>G
|
ENSP00000473654.1:n.*1172C>G
|
|
NM_001185118.1:c.1564C>G
|
NP_001172047.1:p.His522Asp
|
|
NM_001185119.1:c.1483+1142C>G
|
NP_001172048.1:n.1483+1142C>G
|
|
NM_018657.4:c.1564C>G
|
NP_061127.1:p.His522Asp
|
|
NR_033702.1:n.1863C>G
|
|
|
NR_033703.1:n.1877C>G
|
|
|
XM_005247621.3:c.1480C>G
|
XP_005247678.1:p.His494Asp
|
|
XM_005247622.3:c.1318C>G
|
XP_005247679.1:p.His440Asp
|
|
XM_005247624.3:c.1222C>G
|
XP_005247681.1:p.His408Asp
|
|
XM_011512987.1:c.1564C>G
|
XP_011511289.1:p.His522Asp
|
|
XM_011512988.1:c.1564C>G
|
XP_011511290.1:p.His522Asp
|
|
XM_005247621.5:c.1480C>G
|
XP_005247678.1:p.His494Asp
|
|
XM_005247622.4:c.1318C>G
|
XP_005247679.1:p.His440Asp
|
|
XM_005247624.4:c.1222C>G
|
XP_005247681.1:p.His408Asp
|
|
XM_017006864.2:c.1564C>G
|
XP_016862353.1:p.His522Asp
|
|
XM_017006865.2:c.1138C>G
|
XP_016862354.1:p.His380Asp
|
|
XM_017006866.2:c.1138C>G
|
XP_016862355.1:p.His380Asp
|
|
XM_017006867.2:c.745C>G
|
XP_016862356.1:p.His249Asp
|
|
XM_017006868.2:c.661C>G
|
XP_016862357.1:p.His221Asp
|
|
XR_002959552.1:n.3396C>G
|
|
|
NM_001185118.2:c.1564C>G
|
NP_001172047.1:p.His522Asp
|
|
NM_018657.5:c.1564C>G
MANE Select
|
NP_061127.1:p.His522Asp
|
|
NR_033702.2:n.1532C>G
|
|
|
NR_033703.2:n.1546C>G
|
|
|