ENST00000588328.7:c.832G>T
|
ENSP00000468516.4:p.Gly278Cys
|
|
ENST00000651901.2:c.832G>T
|
ENSP00000498922.2:p.Gly278Cys
|
|
ENST00000698359.1:c.787G>T
|
ENSP00000513682.1:p.Gly263Cys
|
|
ENST00000698360.1:c.883G>T
|
ENSP00000513683.1:p.Gly295Cys
|
|
ENST00000698361.1:c.832G>T
|
ENSP00000513684.1:p.Gly278Cys
|
|
ENST00000698362.1:c.832G>T
|
ENSP00000513685.1:p.Gly278Cys
|
|
ENST00000698363.1:n.895G>T
|
|
|
ENST00000698364.1:n.895G>T
|
|
|
ENST00000698365.1:n.895G>T
|
|
|
ENST00000698426.1:c.511G>T
|
ENSP00000513713.1:p.Gly171Cys
|
|
ENST00000698427.1:c.874G>T
|
ENSP00000513714.1:p.Gly292Cys
|
|
ENST00000698428.1:c.511G>T
|
ENSP00000513715.1:p.Gly171Cys
|
|
ENST00000698429.1:n.715G>T
|
|
|
ENST00000698430.1:c.1082G>T
|
|
|
ENST00000698431.1:c.569G>T
|
ENSP00000513717.1:n.569G>T
|
|
ENST00000698432.1:c.641G>T
|
|
|
ENST00000698433.1:n.294G>T
|
|
|
ENST00000698434.1:n.319G>T
|
|
|
ENST00000698435.1:c.520G>T
|
ENSP00000513719.1:p.Gly174Cys
|
|
ENST00000244137.12:c.832G>T
MANE Select
|
ENSP00000244137.5:p.Gly278Cys
|
|
ENST00000588328.6:c.821G>T
|
|
|
ENST00000590731.6:n.507G>T
|
|
|
ENST00000651901.1:c.828G>T
|
|
|
ENST00000244137.11:c.832G>T
|
ENSP00000244137.5:p.Gly278Cys
|
|
ENST00000397032.8:c.709G>T
|
ENSP00000380226.3:p.Gly237Cys
|
|
ENST00000436370.7:c.640G>T
|
ENSP00000391890.2:p.Gly214Cys
|
|
ENST00000588328.5:c.323G>T
|
|
|
ENST00000588719.5:n.467G>T
|
|
|
ENST00000590731.5:n.507G>T
|
|
|
ENST00000593163.5:n.997G>T
|
|
|
ENST00000609145.5:c.265G>T
|
ENSP00000476514.1:p.Gly89Cys
|
|
NM_000285.3:c.832G>T
|
NP_000276.2:p.Gly278Cys
|
|
NM_001166056.1:c.709G>T
|
NP_001159528.1:p.Gly237Cys
|
|
NM_001166057.1:c.640G>T
|
NP_001159529.1:p.Gly214Cys
|
|
NM_000285.4:c.832G>T
MANE Select
|
NP_000276.2:p.Gly278Cys
|
|
NM_001166056.2:c.709G>T
|
NP_001159528.1:p.Gly237Cys
|
|
NM_001166057.2:c.640G>T
|
NP_001159529.1:p.Gly214Cys
|
|