ENST00000588328.7:c.1420G>T
|
ENSP00000468516.4:p.Glu474Ter
|
|
ENST00000651901.2:c.1444G>T
|
ENSP00000498922.2:p.Glu482Ter
|
|
ENST00000698359.1:c.1309G>T
|
ENSP00000513682.1:p.Glu437Ter
|
|
ENST00000698360.1:c.1405G>T
|
ENSP00000513683.1:p.Glu469Ter
|
|
ENST00000698361.1:c.1470G>T
|
ENSP00000513684.1:p.Ser490=
|
|
ENST00000698362.1:c.*491G>T
|
ENSP00000513685.1:n.*491G>T
|
|
ENST00000698426.1:c.1033G>T
|
ENSP00000513713.1:p.Glu345Ter
|
|
ENST00000698427.1:c.1396G>T
|
ENSP00000513714.1:p.Glu466Ter
|
|
ENST00000698428.1:c.1033G>T
|
ENSP00000513715.1:p.Glu345Ter
|
|
ENST00000698429.1:n.1237G>T
|
|
|
ENST00000698430.1:c.1604G>T
|
|
|
ENST00000698431.1:c.1091G>T
|
ENSP00000513717.1:n.1091G>T
|
|
ENST00000698432.1:c.1163G>T
|
|
|
ENST00000698433.1:n.816G>T
|
|
|
ENST00000244137.12:c.1354G>T
MANE Select
|
ENSP00000244137.5:p.Glu452Ter
|
|
ENST00000588328.6:c.1409G>T
|
|
|
ENST00000651901.1:c.1440G>T
|
|
|
ENST00000244137.11:c.1354G>T
|
ENSP00000244137.5:p.Glu452Ter
|
|
ENST00000397032.8:c.1231G>T
|
ENSP00000380226.3:p.Glu411Ter
|
|
ENST00000436370.7:c.1162G>T
|
ENSP00000391890.2:p.Glu388Ter
|
|
ENST00000589598.5:n.79G>T
|
|
|
ENST00000591968.1:n.426G>T
|
|
|
ENST00000593085.1:n.1241G>T
|
|
|
NM_000285.3:c.1354G>T
|
NP_000276.2:p.Glu452Ter
|
|
NM_001166056.1:c.1231G>T
|
NP_001159528.1:p.Glu411Ter
|
|
NM_001166057.1:c.1162G>T
|
NP_001159529.1:p.Glu388Ter
|
|
NM_000285.4:c.1354G>T
MANE Select
|
NP_000276.2:p.Glu452Ter
|
|
NM_001166056.2:c.1231G>T
|
NP_001159528.1:p.Glu411Ter
|
|
NM_001166057.2:c.1162G>T
|
NP_001159529.1:p.Glu388Ter
|
|