ENST00000700029.2:c.1216G>T
|
ENSP00000514759.2:p.Asp406Tyr
|
|
ENST00000710265.1:c.*152G>T
|
ENSP00000518161.1:n.*152G>T
|
|
ENST00000688158.2:n.1858G>T
|
|
|
ENST00000688922.2:c.*953G>T
|
ENSP00000508742.2:n.*953G>T
|
|
ENST00000700021.1:c.1078G>T
|
ENSP00000514757.1:p.Asp360Tyr
|
|
ENST00000700022.1:c.*462G>T
|
ENSP00000514758.1:n.*462G>T
|
|
ENST00000700023.1:n.2281G>T
|
|
|
ENST00000700024.1:n.2515G>T
|
|
|
ENST00000706954.1:c.1123G>T
|
ENSP00000516674.1:p.Asp375Tyr
|
|
ENST00000706955.1:c.*1158G>T
|
ENSP00000516675.1:n.*1158G>T
|
|
ENST00000686459.1:c.*709G>T
|
ENSP00000508909.1:n.*709G>T
|
|
ENST00000688158.1:c.*1234G>T
|
ENSP00000509254.1:n.*1234G>T
|
|
ENST00000688308.1:c.1123G>T
|
ENSP00000508752.1:p.Asp375Tyr
|
|
ENST00000688922.1:c.1044G>T
|
|
|
ENST00000693560.1:c.1642G>T
|
ENSP00000509861.1:p.Asp548Tyr
|
|
ENST00000371953.8:c.1123G>T
MANE Select
|
ENSP00000361021.3:p.Asp375Tyr
|
|
ENST00000371953.7:c.1123G>T
|
ENSP00000361021.3:p.Asp375Tyr
|
|
NM_000314.5:c.1123G>T
|
NP_000305.3:p.Asp375Tyr
|
|
NM_000314.6:c.1123G>T
|
NP_000305.3:p.Asp375Tyr
|
|
NM_001304717.2:c.1642G>T
|
NP_001291646.2:p.Asp548Tyr
|
|
NM_001304718.1:c.532G>T
|
NP_001291647.1:p.Asp178Tyr
|
|
XM_006717926.2:c.1078G>T
|
XP_006717989.1:p.Asp360Tyr
|
|
XM_011539982.1:c.1027G>T
|
XP_011538284.1:p.Asp343Tyr
|
|
XR_945791.1:n.1693G>T
|
|
|
NM_000314.7:c.1123G>T
|
NP_000305.3:p.Asp375Tyr
|
|
NM_001304717.5:c.1642G>T
|
NP_001291646.4:p.Asp548Tyr
|
|
NM_001304718.2:c.532G>T
|
NP_001291647.1:p.Asp178Tyr
|
|
NM_000314.8:c.1123G>T
MANE Select
|
NP_000305.3:p.Asp375Tyr
|
|