ENST00000361740.9:c.825A>C
|
ENSP00000354468.5:p.Ala275=
|
|
ENST00000402438.6:c.624A>C
|
ENSP00000385679.1:p.Ala208=
|
|
ENST00000407332.6:c.711A>C
|
ENSP00000384457.2:p.Ala237=
|
|
ENST00000407623.8:c.624A>C
|
ENSP00000384834.3:p.Ala208=
|
|
ENST00000617178.5:c.230A>C
|
|
|
ENST00000684963.1:n.2433A>C
|
|
|
ENST00000685184.1:n.285A>C
|
|
|
ENST00000686523.1:c.*642A>C
|
ENSP00000508940.1:n.*642A>C
|
|
ENST00000687183.1:n.969A>C
|
|
|
ENST00000687198.1:c.624A>C
|
ENSP00000508492.1:p.Ala208=
|
|
ENST00000688117.1:c.792A>C
|
ENSP00000509015.1:p.Ala264=
|
|
ENST00000688244.1:c.393A>C
|
ENSP00000510355.1:p.Ala131=
|
|
ENST00000689001.1:n.1315A>C
|
|
|
ENST00000689195.1:c.609A>C
|
ENSP00000509895.1:p.Ala203=
|
|
ENST00000689239.1:n.860A>C
|
|
|
ENST00000689795.1:n.954A>C
|
|
|
ENST00000690835.1:c.*72A>C
|
ENSP00000509038.1:n.*72A>C
|
|
ENST00000690993.1:n.1448A>C
|
|
|
ENST00000691295.1:c.*176A>C
|
ENSP00000508706.1:n.*176A>C
|
|
ENST00000691918.1:c.983A>C
|
ENSP00000509525.1:n.983A>C
|
|
ENST00000692152.1:c.624A>C
|
ENSP00000509317.1:p.Ala208=
|
|
ENST00000692344.1:n.1180A>C
|
|
|
ENST00000693363.1:c.735A>C
|
ENSP00000510411.1:p.Ala245=
|
|
ENST00000693367.1:c.693A>C
|
ENSP00000508815.1:p.Ala231=
|
|
ENST00000693639.1:c.686A>C
|
ENSP00000510223.1:n.686A>C
|
|
ENST00000693646.1:c.599A>C
|
ENSP00000508449.1:n.599A>C
|
|
ENST00000352397.10:c.693A>C
MANE Select
|
ENSP00000338461.6:p.Ala231=
|
|
ENST00000352397.9:c.693A>C
|
ENSP00000338461.6:p.Ala231=
|
|
ENST00000361740.8:c.792A>C
|
ENSP00000354468.4:p.Ala264=
|
|
ENST00000402438.5:c.624A>C
|
ENSP00000385679.1:p.Ala208=
|
|
ENST00000407332.5:c.624A>C
|
ENSP00000384457.1:p.Ala208=
|
|
ENST00000407623.7:c.624A>C
|
ENSP00000384834.3:p.Ala208=
|
|
ENST00000470741.1:n.2827A>C
|
|
|
NM_000398.6:c.693A>C
|
NP_000389.1:p.Ala231=
|
|
NM_001129819.2:c.624A>C
|
NP_001123291.1:p.Ala208=
|
|
NM_001171660.1:c.792A>C
|
NP_001165131.1:p.Ala264=
|
|
NM_001171661.1:c.624A>C
|
NP_001165132.1:p.Ala208=
|
|
NM_007326.4:c.624A>C
|
NP_015565.1:p.Ala208=
|
|
NM_000398.7:c.693A>C
MANE Select
|
NP_000389.1:p.Ala231=
|
|
NM_001171660.2:c.792A>C
|
NP_001165131.1:p.Ala264=
|
|