ENST00000703783.1:n.1078T>G
|
|
|
ENST00000703785.1:n.1159T>G
|
|
|
ENST00000262464.9:c.4294T>G
MANE Select
|
ENSP00000262464.4:p.Tyr1432Asp
|
|
ENST00000262464.8:c.4294T>G
|
ENSP00000262464.4:p.Tyr1432Asp
|
|
ENST00000507835.5:c.844T>G
|
ENSP00000426839.1:p.Tyr282Asp
|
|
ENST00000508053.5:c.4294T>G
|
ENSP00000424571.1:p.Tyr1432Asp
|
|
ENST00000508989.5:c.4195T>G
|
ENSP00000425596.1:p.Tyr1399Asp
|
|
ENST00000619499.4:c.4291T>G
|
ENSP00000482132.1:p.Tyr1431Asp
|
|
NM_001999.3:c.4294T>G
|
NP_001990.2:p.Tyr1432Asp
|
|
XM_017009228.2:c.4141T>G
|
XP_016864717.1:p.Tyr1381Asp
|
|
NM_001999.4:c.4294T>G
MANE Select
|
NP_001990.2:p.Tyr1432Asp
|
|