ENST00000682338.1:c.1737T>G
|
ENSP00000507062.1:p.Tyr579Ter
|
|
ENST00000682793.1:c.1737T>G
|
ENSP00000506910.1:p.Tyr579Ter
|
|
ENST00000682838.1:c.*1479T>G
|
ENSP00000507652.1:n.*1479T>G
|
|
ENST00000683578.1:c.1737T>G
|
ENSP00000507430.1:p.Tyr579Ter
|
|
ENST00000683606.1:n.1343T>G
|
|
|
ENST00000683661.1:n.3272T>G
|
|
|
ENST00000684324.1:c.1737T>G
|
ENSP00000507937.1:p.Tyr579Ter
|
|
ENST00000684545.1:c.1737T>G
|
ENSP00000506733.1:p.Tyr579Ter
|
|
ENST00000684624.1:n.1114T>G
|
|
|
ENST00000684714.1:c.1707+30T>G
|
ENSP00000506861.1:n.1707+30T>G
|
|
ENST00000684731.1:n.1083+1342T>G
|
|
|
ENST00000375679.9:c.1737T>G
MANE Select
|
ENSP00000364831.5:p.Tyr579Ter
|
|
ENST00000375667.7:c.1230T>G
|
ENSP00000364819.3:p.Tyr410Ter
|
|
ENST00000375679.8:c.1737T>G
|
ENSP00000364831.4:p.Tyr579Ter
|
|
ENST00000431772.1:c.204T>G
|
ENSP00000389344.1:p.Tyr68Ter
|
|
ENST00000619181.4:c.1293+63T>G
|
ENSP00000483866.1:n.1293+63T>G
|
|
NM_000085.4:c.1737T>G
|
NP_000076.2:p.Tyr579Ter
|
|
NM_001165945.2:c.1230T>G
|
NP_001159417.2:p.Tyr410Ter
|
|
XM_011540619.1:c.1578T>G
|
XP_011538921.1:p.Tyr526Ter
|
|
XM_011540621.1:c.1086T>G
|
XP_011538923.1:p.Tyr362Ter
|
|
NM_000085.5:c.1737T>G
MANE Select
|
NP_000076.2:p.Tyr579Ter
|
|