ENST00000682424.1:c.1255G>T
|
ENSP00000507321.1:p.Asp419Tyr
|
|
ENST00000299427.12:c.1369G>T
MANE Select
|
ENSP00000299427.6:p.Asp457Tyr
|
|
ENST00000524611.2:n.229G>T
|
|
|
ENST00000524924.2:n.489G>T
|
|
|
ENST00000533371.6:c.640G>T
|
ENSP00000437066.1:p.Asp214Tyr
|
|
ENST00000642892.1:c.640G>T
|
ENSP00000494165.1:p.Asp214Tyr
|
|
ENST00000643342.1:c.442G>T
|
|
|
ENST00000643439.1:c.*1109G>T
|
ENSP00000495849.1:n.*1109G>T
|
|
ENST00000643479.1:n.1555G>T
|
|
|
ENST00000643516.1:c.878G>T
|
|
|
ENST00000644218.1:c.1180G>T
|
ENSP00000493574.1:p.Asp394Tyr
|
|
ENST00000644683.1:c.*822G>T
|
ENSP00000494085.1:n.*822G>T
|
|
ENST00000644810.1:c.1090G>T
|
ENSP00000495895.1:p.Asp364Tyr
|
|
ENST00000644831.1:n.1545G>T
|
|
|
ENST00000644933.1:c.*235G>T
|
ENSP00000496133.1:n.*235G>T
|
|
ENST00000645285.1:c.*235G>T
|
ENSP00000495058.1:n.*235G>T
|
|
ENST00000645331.1:n.2574G>T
|
|
|
ENST00000645620.1:c.640G>T
|
ENSP00000493657.1:p.Asp214Tyr
|
|
ENST00000646691.1:n.1256G>T
|
|
|
ENST00000646777.1:n.1702G>T
|
|
|
ENST00000647016.1:n.1849G>T
|
|
|
ENST00000647152.1:c.640G>T
|
ENSP00000495893.1:p.Asp214Tyr
|
|
ENST00000647209.1:c.*1238G>T
|
ENSP00000495558.1:n.*1238G>T
|
|
ENST00000647346.1:n.2389G>T
|
|
|
ENST00000299427.10:c.1369G>T
|
ENSP00000299427.6:p.Asp457Tyr
|
|
ENST00000524611.1:n.247G>T
|
|
|
ENST00000532191.1:n.422G>T
|
|
|
ENST00000533371.5:c.640G>T
|
ENSP00000437066.1:p.Asp214Tyr
|
|
ENST00000611494.4:c.1369G>T
|
ENSP00000484546.1:p.Asp457Tyr
|
|
NM_000391.3:c.1369G>T
|
NP_000382.3:p.Asp457Tyr
|
|
NM_000391.4:c.1369G>T
MANE Select
|
NP_000382.3:p.Asp457Tyr
|
|