ENST00000588328.7:c.1438A=
|
ENSP00000468516.4:p.Thr480=
|
|
ENST00000651901.2:c.1462A=
|
ENSP00000498922.2:p.Thr488=
|
|
ENST00000698359.1:c.1327A=
|
ENSP00000513682.1:p.Thr443=
|
|
ENST00000698360.1:c.1423A=
|
ENSP00000513683.1:p.Thr475=
|
|
ENST00000698361.1:c.1488A=
|
ENSP00000513684.1:p.Ter496=
|
|
ENST00000698362.1:c.*509A=
|
ENSP00000513685.1:n.*509A=
|
|
ENST00000698426.1:c.1051A=
|
ENSP00000513713.1:p.Thr351=
|
|
ENST00000698427.1:c.1414A=
|
ENSP00000513714.1:p.Thr472=
|
|
ENST00000698428.1:c.1051A=
|
ENSP00000513715.1:p.Thr351=
|
|
ENST00000698429.1:n.1255A=
|
|
|
ENST00000698430.1:c.1622A=
|
|
|
ENST00000698431.1:c.1109A=
|
ENSP00000513717.1:n.1109A=
|
|
ENST00000698432.1:c.1181A=
|
|
|
ENST00000698433.1:n.834A=
|
|
|
ENST00000244137.12:c.1372A=
MANE Select
|
ENSP00000244137.5:p.Thr458=
|
|
ENST00000588328.6:c.1427A=
|
|
|
ENST00000651901.1:c.1458A=
|
|
|
ENST00000244137.11:c.1372A=
|
ENSP00000244137.5:p.Thr458=
|
|
ENST00000397032.8:c.1249A=
|
ENSP00000380226.3:p.Thr417=
|
|
ENST00000436370.7:c.1180A=
|
ENSP00000391890.2:p.Thr394=
|
|
ENST00000589598.5:n.97A=
|
|
|
ENST00000591968.1:n.444A=
|
|
|
ENST00000593085.1:n.1259A=
|
|
|
NM_000285.3:c.1372A=
|
NP_000276.2:p.Thr458=
|
|
NM_001166056.1:c.1249A=
|
NP_001159528.1:p.Thr417=
|
|
NM_001166057.1:c.1180A=
|
NP_001159529.1:p.Thr394=
|
|
NM_000285.4:c.1372A=
MANE Select
|
NP_000276.2:p.Thr458=
|
|
NM_001166056.2:c.1249A=
|
NP_001159528.1:p.Thr417=
|
|
NM_001166057.2:c.1180A=
|
NP_001159529.1:p.Thr394=
|
|