ENST00000682424.1:c.1231T>G
|
ENSP00000507321.1:p.Tyr411Asp
|
|
ENST00000299427.12:c.1345T>G
MANE Select
|
ENSP00000299427.6:p.Tyr449Asp
|
|
ENST00000524611.2:n.205T>G
|
|
|
ENST00000524924.2:n.465T>G
|
|
|
ENST00000533371.6:c.616T>G
|
ENSP00000437066.1:p.Tyr206Asp
|
|
ENST00000642892.1:c.616T>G
|
ENSP00000494165.1:p.Tyr206Asp
|
|
ENST00000643342.1:c.418T>G
|
|
|
ENST00000643439.1:c.*1085T>G
|
ENSP00000495849.1:n.*1085T>G
|
|
ENST00000643479.1:n.1531T>G
|
|
|
ENST00000643516.1:c.854T>G
|
|
|
ENST00000644218.1:c.1156T>G
|
ENSP00000493574.1:p.Tyr386Asp
|
|
ENST00000644683.1:c.*798T>G
|
ENSP00000494085.1:n.*798T>G
|
|
ENST00000644810.1:c.1066T>G
|
ENSP00000495895.1:p.Tyr356Asp
|
|
ENST00000644831.1:n.1521T>G
|
|
|
ENST00000644933.1:c.*211T>G
|
ENSP00000496133.1:n.*211T>G
|
|
ENST00000645285.1:c.*211T>G
|
ENSP00000495058.1:n.*211T>G
|
|
ENST00000645331.1:n.2550T>G
|
|
|
ENST00000645620.1:c.616T>G
|
ENSP00000493657.1:p.Tyr206Asp
|
|
ENST00000646691.1:n.1232T>G
|
|
|
ENST00000646777.1:n.1678T>G
|
|
|
ENST00000647016.1:n.1825T>G
|
|
|
ENST00000647152.1:c.616T>G
|
ENSP00000495893.1:p.Tyr206Asp
|
|
ENST00000647209.1:c.*1214T>G
|
ENSP00000495558.1:n.*1214T>G
|
|
ENST00000647346.1:n.2365T>G
|
|
|
ENST00000299427.10:c.1345T>G
|
ENSP00000299427.6:p.Tyr449Asp
|
|
ENST00000524611.1:n.223T>G
|
|
|
ENST00000532191.1:n.398T>G
|
|
|
ENST00000533371.5:c.616T>G
|
ENSP00000437066.1:p.Tyr206Asp
|
|
ENST00000611494.4:c.1345T>G
|
ENSP00000484546.1:p.Tyr449Asp
|
|
NM_000391.3:c.1345T>G
|
NP_000382.3:p.Tyr449Asp
|
|
NM_000391.4:c.1345T>G
MANE Select
|
NP_000382.3:p.Tyr449Asp
|
|