ENST00000682424.1:c.1147T>G
|
ENSP00000507321.1:p.Tyr383Asp
|
|
ENST00000299427.12:c.1261T>G
MANE Select
|
ENSP00000299427.6:p.Tyr421Asp
|
|
ENST00000436873.7:c.498T>G
|
|
|
ENST00000524611.2:n.9T>G
|
|
|
ENST00000524924.2:n.381T>G
|
|
|
ENST00000533371.6:c.532T>G
|
ENSP00000437066.1:p.Tyr178Asp
|
|
ENST00000642892.1:c.532T>G
|
ENSP00000494165.1:p.Tyr178Asp
|
|
ENST00000643342.1:c.334T>G
|
|
|
ENST00000643439.1:c.*1001T>G
|
ENSP00000495849.1:n.*1001T>G
|
|
ENST00000643479.1:n.1447T>G
|
|
|
ENST00000643516.1:c.770T>G
|
|
|
ENST00000644218.1:c.1072T>G
|
ENSP00000493574.1:p.Tyr358Asp
|
|
ENST00000644683.1:c.*714T>G
|
ENSP00000494085.1:n.*714T>G
|
|
ENST00000644810.1:c.982T>G
|
ENSP00000495895.1:p.Tyr328Asp
|
|
ENST00000644831.1:n.1437T>G
|
|
|
ENST00000644933.1:c.*127T>G
|
ENSP00000496133.1:n.*127T>G
|
|
ENST00000645285.1:c.*127T>G
|
ENSP00000495058.1:n.*127T>G
|
|
ENST00000645331.1:n.2466T>G
|
|
|
ENST00000645620.1:c.532T>G
|
ENSP00000493657.1:p.Tyr178Asp
|
|
ENST00000646691.1:n.1036T>G
|
|
|
ENST00000646777.1:n.1594T>G
|
|
|
ENST00000647016.1:n.1741T>G
|
|
|
ENST00000647152.1:c.532T>G
|
ENSP00000495893.1:p.Tyr178Asp
|
|
ENST00000647209.1:c.*1130T>G
|
ENSP00000495558.1:n.*1130T>G
|
|
ENST00000647346.1:n.2281T>G
|
|
|
ENST00000299427.10:c.1261T>G
|
ENSP00000299427.6:p.Tyr421Asp
|
|
ENST00000524611.1:n.27T>G
|
|
|
ENST00000524924.1:n.216T>G
|
|
|
ENST00000532191.1:n.314T>G
|
|
|
ENST00000533371.5:c.532T>G
|
ENSP00000437066.1:p.Tyr178Asp
|
|
ENST00000611494.4:c.1261T>G
|
ENSP00000484546.1:p.Tyr421Asp
|
|
NM_000391.3:c.1261T>G
|
NP_000382.3:p.Tyr421Asp
|
|
NM_000391.4:c.1261T>G
MANE Select
|
NP_000382.3:p.Tyr421Asp
|
|