ENST00000700029.2:c.1249G>T
|
ENSP00000514759.2:p.Asp417Tyr
|
|
ENST00000710265.1:c.*185G>T
|
ENSP00000518161.1:n.*185G>T
|
|
ENST00000688158.2:n.1891G>T
|
|
|
ENST00000688922.2:c.*986G>T
|
ENSP00000508742.2:n.*986G>T
|
|
ENST00000700021.1:c.1111G>T
|
ENSP00000514757.1:p.Asp371Tyr
|
|
ENST00000700022.1:c.*495G>T
|
ENSP00000514758.1:n.*495G>T
|
|
ENST00000700023.1:n.2314G>T
|
|
|
ENST00000700024.1:n.2548G>T
|
|
|
ENST00000706954.1:c.1156G>T
|
ENSP00000516674.1:p.Asp386Tyr
|
|
ENST00000706955.1:c.*1191G>T
|
ENSP00000516675.1:n.*1191G>T
|
|
ENST00000686459.1:c.*742G>T
|
ENSP00000508909.1:n.*742G>T
|
|
ENST00000688158.1:c.*1267G>T
|
ENSP00000509254.1:n.*1267G>T
|
|
ENST00000688308.1:c.1156G>T
|
ENSP00000508752.1:p.Asp386Tyr
|
|
ENST00000688922.1:c.1077G>T
|
|
|
ENST00000693560.1:c.1675G>T
|
ENSP00000509861.1:p.Asp559Tyr
|
|
ENST00000371953.8:c.1156G>T
MANE Select
|
ENSP00000361021.3:p.Asp386Tyr
|
|
ENST00000371953.7:c.1156G>T
|
ENSP00000361021.3:p.Asp386Tyr
|
|
NM_000314.5:c.1156G>T
|
NP_000305.3:p.Asp386Tyr
|
|
NM_000314.6:c.1156G>T
|
NP_000305.3:p.Asp386Tyr
|
|
NM_001304717.2:c.1675G>T
|
NP_001291646.2:p.Asp559Tyr
|
|
NM_001304718.1:c.565G>T
|
NP_001291647.1:p.Asp189Tyr
|
|
XM_006717926.2:c.1111G>T
|
XP_006717989.1:p.Asp371Tyr
|
|
XM_011539982.1:c.1060G>T
|
XP_011538284.1:p.Asp354Tyr
|
|
XR_945791.1:n.1726G>T
|
|
|
NM_000314.7:c.1156G>T
|
NP_000305.3:p.Asp386Tyr
|
|
NM_001304717.5:c.1675G>T
|
NP_001291646.4:p.Asp559Tyr
|
|
NM_001304718.2:c.565G>T
|
NP_001291647.1:p.Asp189Tyr
|
|
NM_000314.8:c.1156G>T
MANE Select
|
NP_000305.3:p.Asp386Tyr
|
|