ENST00000588328.7:c.1481T>G
|
ENSP00000468516.4:p.Val494Gly
|
|
ENST00000651901.2:c.1505T>G
|
ENSP00000498922.2:p.Val502Gly
|
|
ENST00000698359.1:c.1370T>G
|
ENSP00000513682.1:p.Val457Gly
|
|
ENST00000698360.1:c.1466T>G
|
ENSP00000513683.1:p.Val489Gly
|
|
ENST00000698361.1:c.*43T>G
|
ENSP00000513684.1:n.*43T>G
|
|
ENST00000698362.1:c.*552T>G
|
ENSP00000513685.1:n.*552T>G
|
|
ENST00000698426.1:c.1094T>G
|
ENSP00000513713.1:p.Val365Gly
|
|
ENST00000698427.1:c.1457T>G
|
ENSP00000513714.1:p.Val486Gly
|
|
ENST00000698428.1:c.1094T>G
|
ENSP00000513715.1:p.Val365Gly
|
|
ENST00000698429.1:n.1298T>G
|
|
|
ENST00000698430.1:c.1665T>G
|
|
|
ENST00000698431.1:c.1152T>G
|
ENSP00000513717.1:n.1152T>G
|
|
ENST00000698432.1:c.1224T>G
|
|
|
ENST00000698433.1:n.877T>G
|
|
|
ENST00000244137.12:c.1415T>G
MANE Select
|
ENSP00000244137.5:p.Val472Gly
|
|
ENST00000588328.6:c.1470T>G
|
|
|
ENST00000651901.1:c.1501T>G
|
|
|
ENST00000244137.11:c.1415T>G
|
ENSP00000244137.5:p.Val472Gly
|
|
ENST00000397032.8:c.1292T>G
|
ENSP00000380226.3:p.Val431Gly
|
|
ENST00000436370.7:c.1223T>G
|
ENSP00000391890.2:p.Val408Gly
|
|
ENST00000589598.5:n.140T>G
|
|
|
ENST00000591968.1:n.487T>G
|
|
|
ENST00000593085.1:n.1302T>G
|
|
|
NM_000285.3:c.1415T>G
|
NP_000276.2:p.Val472Gly
|
|
NM_001166056.1:c.1292T>G
|
NP_001159528.1:p.Val431Gly
|
|
NM_001166057.1:c.1223T>G
|
NP_001159529.1:p.Val408Gly
|
|
NM_000285.4:c.1415T>G
MANE Select
|
NP_000276.2:p.Val472Gly
|
|
NM_001166056.2:c.1292T>G
|
NP_001159528.1:p.Val431Gly
|
|
NM_001166057.2:c.1223T>G
|
NP_001159529.1:p.Val408Gly
|
|