ENST00000682424.1:c.1495T>G
|
ENSP00000507321.1:p.Cys499Gly
|
|
ENST00000299427.12:c.1609T>G
MANE Select
|
ENSP00000299427.6:p.Cys537Gly
|
|
ENST00000524611.2:n.648T>G
|
|
|
ENST00000524924.2:n.729T>G
|
|
|
ENST00000533371.6:c.880T>G
|
ENSP00000437066.1:p.Cys294Gly
|
|
ENST00000642892.1:c.880T>G
|
ENSP00000494165.1:p.Cys294Gly
|
|
ENST00000643342.1:c.682T>G
|
|
|
ENST00000643439.1:c.*1349T>G
|
ENSP00000495849.1:n.*1349T>G
|
|
ENST00000643479.1:n.1795T>G
|
|
|
ENST00000643516.1:c.1118T>G
|
|
|
ENST00000644218.1:c.1420T>G
|
ENSP00000493574.1:p.Cys474Gly
|
|
ENST00000644683.1:c.*1062T>G
|
ENSP00000494085.1:n.*1062T>G
|
|
ENST00000644810.1:c.1330T>G
|
ENSP00000495895.1:p.Cys444Gly
|
|
ENST00000644831.1:n.1785T>G
|
|
|
ENST00000644933.1:c.*475T>G
|
ENSP00000496133.1:n.*475T>G
|
|
ENST00000645285.1:c.*475T>G
|
ENSP00000495058.1:n.*475T>G
|
|
ENST00000645331.1:n.2814T>G
|
|
|
ENST00000645620.1:c.880T>G
|
ENSP00000493657.1:p.Cys294Gly
|
|
ENST00000646691.1:n.1496T>G
|
|
|
ENST00000646777.1:n.1942T>G
|
|
|
ENST00000647016.1:n.2089T>G
|
|
|
ENST00000647152.1:c.880T>G
|
ENSP00000495893.1:p.Cys294Gly
|
|
ENST00000647209.1:c.*1478T>G
|
ENSP00000495558.1:n.*1478T>G
|
|
ENST00000647346.1:n.2629T>G
|
|
|
ENST00000299427.10:c.1609T>G
|
ENSP00000299427.6:p.Cys537Gly
|
|
ENST00000533371.5:c.880T>G
|
ENSP00000437066.1:p.Cys294Gly
|
|
ENST00000611494.4:c.1609T>G
|
ENSP00000484546.1:p.Cys537Gly
|
|
NM_000391.3:c.1609T>G
|
NP_000382.3:p.Cys537Gly
|
|
NM_000391.4:c.1609T>G
MANE Select
|
NP_000382.3:p.Cys537Gly
|
|