ENST00000361740.9:c.841T>G
|
ENSP00000354468.5:p.Tyr281Asp
|
|
ENST00000402438.6:c.640T>G
|
ENSP00000385679.1:p.Tyr214Asp
|
|
ENST00000407332.6:c.727T>G
|
ENSP00000384457.2:p.Tyr243Asp
|
|
ENST00000407623.8:c.640T>G
|
ENSP00000384834.3:p.Tyr214Asp
|
|
ENST00000617178.5:c.246T>G
|
|
|
ENST00000684963.1:n.2449T>G
|
|
|
ENST00000685184.1:n.301T>G
|
|
|
ENST00000686523.1:c.*658T>G
|
ENSP00000508940.1:n.*658T>G
|
|
ENST00000687183.1:n.985T>G
|
|
|
ENST00000687198.1:c.640T>G
|
ENSP00000508492.1:p.Tyr214Asp
|
|
ENST00000688117.1:c.808T>G
|
ENSP00000509015.1:p.Tyr270Asp
|
|
ENST00000688244.1:c.409T>G
|
ENSP00000510355.1:p.Tyr137Asp
|
|
ENST00000689001.1:n.1331T>G
|
|
|
ENST00000689195.1:c.625T>G
|
ENSP00000509895.1:p.Tyr209Asp
|
|
ENST00000689239.1:n.876T>G
|
|
|
ENST00000689795.1:n.970T>G
|
|
|
ENST00000690835.1:c.*88T>G
|
ENSP00000509038.1:n.*88T>G
|
|
ENST00000690993.1:n.1464T>G
|
|
|
ENST00000691295.1:c.*192T>G
|
ENSP00000508706.1:n.*192T>G
|
|
ENST00000691918.1:c.999T>G
|
ENSP00000509525.1:n.999T>G
|
|
ENST00000692152.1:c.640T>G
|
ENSP00000509317.1:p.Tyr214Asp
|
|
ENST00000692344.1:n.1196T>G
|
|
|
ENST00000693363.1:c.751T>G
|
ENSP00000510411.1:p.Tyr251Asp
|
|
ENST00000693367.1:c.709T>G
|
ENSP00000508815.1:p.Tyr237Asp
|
|
ENST00000693639.1:c.702T>G
|
ENSP00000510223.1:n.702T>G
|
|
ENST00000693646.1:c.615T>G
|
ENSP00000508449.1:n.615T>G
|
|
ENST00000352397.10:c.709T>G
MANE Select
|
ENSP00000338461.6:p.Tyr237Asp
|
|
ENST00000352397.9:c.709T>G
|
ENSP00000338461.6:p.Tyr237Asp
|
|
ENST00000361740.8:c.808T>G
|
ENSP00000354468.4:p.Tyr270Asp
|
|
ENST00000402438.5:c.640T>G
|
ENSP00000385679.1:p.Tyr214Asp
|
|
ENST00000407332.5:c.640T>G
|
ENSP00000384457.1:p.Tyr214Asp
|
|
ENST00000407623.7:c.640T>G
|
ENSP00000384834.3:p.Tyr214Asp
|
|
ENST00000470741.1:n.2843T>G
|
|
|
NM_000398.6:c.709T>G
|
NP_000389.1:p.Tyr237Asp
|
|
NM_001129819.2:c.640T>G
|
NP_001123291.1:p.Tyr214Asp
|
|
NM_001171660.1:c.808T>G
|
NP_001165131.1:p.Tyr270Asp
|
|
NM_001171661.1:c.640T>G
|
NP_001165132.1:p.Tyr214Asp
|
|
NM_007326.4:c.640T>G
|
NP_015565.1:p.Tyr214Asp
|
|
NM_000398.7:c.709T>G
MANE Select
|
NP_000389.1:p.Tyr237Asp
|
|
NM_001171660.2:c.808T>G
|
NP_001165131.1:p.Tyr270Asp
|
|