ENST00000361740.9:c.824C>A
|
ENSP00000354468.5:p.Ala275Glu
|
|
ENST00000402438.6:c.623C>A
|
ENSP00000385679.1:p.Ala208Glu
|
|
ENST00000407332.6:c.710C>A
|
ENSP00000384457.2:p.Ala237Glu
|
|
ENST00000407623.8:c.623C>A
|
ENSP00000384834.3:p.Ala208Glu
|
|
ENST00000617178.5:c.229C>A
|
|
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ENST00000684963.1:n.2432C>A
|
|
|
ENST00000685184.1:n.284C>A
|
|
|
ENST00000686523.1:c.*641C>A
|
ENSP00000508940.1:n.*641C>A
|
|
ENST00000687183.1:n.968C>A
|
|
|
ENST00000687198.1:c.623C>A
|
ENSP00000508492.1:p.Ala208Glu
|
|
ENST00000688117.1:c.791C>A
|
ENSP00000509015.1:p.Ala264Glu
|
|
ENST00000688244.1:c.392C>A
|
ENSP00000510355.1:p.Ala131Glu
|
|
ENST00000689001.1:n.1314C>A
|
|
|
ENST00000689195.1:c.608C>A
|
ENSP00000509895.1:p.Ala203Glu
|
|
ENST00000689239.1:n.859C>A
|
|
|
ENST00000689795.1:n.953C>A
|
|
|
ENST00000690835.1:c.*71C>A
|
ENSP00000509038.1:n.*71C>A
|
|
ENST00000690993.1:n.1447C>A
|
|
|
ENST00000691295.1:c.*175C>A
|
ENSP00000508706.1:n.*175C>A
|
|
ENST00000691918.1:c.982C>A
|
ENSP00000509525.1:n.982C>A
|
|
ENST00000692152.1:c.623C>A
|
ENSP00000509317.1:p.Ala208Glu
|
|
ENST00000692344.1:n.1179C>A
|
|
|
ENST00000693363.1:c.734C>A
|
ENSP00000510411.1:p.Ala245Glu
|
|
ENST00000693367.1:c.692C>A
|
ENSP00000508815.1:p.Ala231Glu
|
|
ENST00000693639.1:c.685C>A
|
ENSP00000510223.1:n.685C>A
|
|
ENST00000693646.1:c.598C>A
|
ENSP00000508449.1:n.598C>A
|
|
ENST00000352397.10:c.692C>A
MANE Select
|
ENSP00000338461.6:p.Ala231Glu
|
|
ENST00000352397.9:c.692C>A
|
ENSP00000338461.6:p.Ala231Glu
|
|
ENST00000361740.8:c.791C>A
|
ENSP00000354468.4:p.Ala264Glu
|
|
ENST00000402438.5:c.623C>A
|
ENSP00000385679.1:p.Ala208Glu
|
|
ENST00000407332.5:c.623C>A
|
ENSP00000384457.1:p.Ala208Glu
|
|
ENST00000407623.7:c.623C>A
|
ENSP00000384834.3:p.Ala208Glu
|
|
ENST00000470741.1:n.2826C>A
|
|
|
NM_000398.6:c.692C>A
|
NP_000389.1:p.Ala231Glu
|
|
NM_001129819.2:c.623C>A
|
NP_001123291.1:p.Ala208Glu
|
|
NM_001171660.1:c.791C>A
|
NP_001165131.1:p.Ala264Glu
|
|
NM_001171661.1:c.623C>A
|
NP_001165132.1:p.Ala208Glu
|
|
NM_007326.4:c.623C>A
|
NP_015565.1:p.Ala208Glu
|
|
NM_000398.7:c.692C>A
MANE Select
|
NP_000389.1:p.Ala231Glu
|
|
NM_001171660.2:c.791C>A
|
NP_001165131.1:p.Ala264Glu
|
|