ENST00000636937.2:c.3378T>G
|
ENSP00000516154.1:p.Asp1126Glu
|
|
ENST00000268124.11:c.3378T>G
MANE Select
|
ENSP00000268124.5:p.Asp1126Glu
|
|
ENST00000530292.3:c.2979T>G
|
ENSP00000432885.2:p.Asp993Glu
|
|
ENST00000635986.2:c.*448T>G
|
ENSP00000490653.2:n.*448T>G
|
|
ENST00000636774.1:c.*1945T>G
|
ENSP00000489799.1:n.*1945T>G
|
|
ENST00000637238.1:c.2187T>G
|
ENSP00000490756.1:n.2187T>G
|
|
ENST00000637264.1:c.2450T>G
|
|
|
ENST00000666746.1:c.2955T>G
|
|
|
ENST00000672071.1:n.3576T>G
|
|
|
ENST00000672695.1:n.555T>G
|
|
|
ENST00000672923.2:n.3378T>G
|
|
|
ENST00000268124.9:c.3378T>G
|
ENSP00000268124.5:p.Asp1126Glu
|
|
ENST00000442287.6:c.3378T>G
|
ENSP00000399851.2:p.Asp1126Glu
|
|
ENST00000530292.2:c.462T>G
|
ENSP00000432885.1:p.Asp154Glu
|
|
ENST00000631044.2:c.*2802T>G
|
ENSP00000486730.1:n.*2802T>G
|
|
NM_001126131.1:c.3378T>G
|
NP_001119603.1:p.Asp1126Glu
|
|
NM_002693.2:c.3378T>G
|
NP_002684.1:p.Asp1126Glu
|
|
NM_001126131.2:c.3378T>G
|
NP_001119603.1:p.Asp1126Glu
|
|
NM_002693.3:c.3378T>G
MANE Select
|
NP_002684.1:p.Asp1126Glu
|
|