ENST00000588328.7:c.826G=
|
ENSP00000468516.4:p.Asp276=
|
|
ENST00000651901.2:c.826G=
|
ENSP00000498922.2:p.Asp276=
|
|
ENST00000698359.1:c.781G=
|
ENSP00000513682.1:p.Asp261=
|
|
ENST00000698360.1:c.877G=
|
ENSP00000513683.1:p.Asp293=
|
|
ENST00000698361.1:c.826G=
|
ENSP00000513684.1:p.Asp276=
|
|
ENST00000698362.1:c.826G=
|
ENSP00000513685.1:p.Asp276=
|
|
ENST00000698363.1:n.889G=
|
|
|
ENST00000698364.1:n.889G=
|
|
|
ENST00000698365.1:n.889G=
|
|
|
ENST00000698426.1:c.505G=
|
ENSP00000513713.1:p.Asp169=
|
|
ENST00000698427.1:c.868G=
|
ENSP00000513714.1:p.Asp290=
|
|
ENST00000698428.1:c.505G=
|
ENSP00000513715.1:p.Asp169=
|
|
ENST00000698429.1:n.709G=
|
|
|
ENST00000698430.1:c.1076G=
|
|
|
ENST00000698431.1:c.563G=
|
ENSP00000513717.1:n.563G=
|
|
ENST00000698432.1:c.635G=
|
|
|
ENST00000698433.1:n.288G=
|
|
|
ENST00000698434.1:n.313G=
|
|
|
ENST00000698435.1:c.514G=
|
ENSP00000513719.1:p.Asp172=
|
|
ENST00000244137.12:c.826G=
MANE Select
|
ENSP00000244137.5:p.Asp276=
|
|
ENST00000588328.6:c.815G=
|
|
|
ENST00000590731.6:n.501G=
|
|
|
ENST00000651901.1:c.822G=
|
|
|
ENST00000244137.11:c.826G=
|
ENSP00000244137.5:p.Asp276=
|
|
ENST00000397032.8:c.703G=
|
ENSP00000380226.3:p.Asp235=
|
|
ENST00000436370.7:c.634G=
|
ENSP00000391890.2:p.Asp212=
|
|
ENST00000588328.5:c.317G=
|
|
|
ENST00000588719.5:n.461G=
|
|
|
ENST00000590731.5:n.501G=
|
|
|
ENST00000593163.5:n.991G=
|
|
|
ENST00000609145.5:c.259G=
|
ENSP00000476514.1:p.Asp87=
|
|
NM_000285.3:c.826G=
|
NP_000276.2:p.Asp276=
|
|
NM_001166056.1:c.703G=
|
NP_001159528.1:p.Asp235=
|
|
NM_001166057.1:c.634G=
|
NP_001159529.1:p.Asp212=
|
|
NM_000285.4:c.826G=
MANE Select
|
NP_000276.2:p.Asp276=
|
|
NM_001166056.2:c.703G=
|
NP_001159528.1:p.Asp235=
|
|
NM_001166057.2:c.634G=
|
NP_001159529.1:p.Asp212=
|
|