ENST00000361740.9:c.232C>G
|
ENSP00000354468.5:p.His78Asp
|
|
ENST00000402438.6:c.163C>G
|
ENSP00000385679.1:p.His55Asp
|
|
ENST00000407332.6:c.250C>G
|
ENSP00000384457.2:p.His84Asp
|
|
ENST00000407623.8:c.163C>G
|
ENSP00000384834.3:p.His55Asp
|
|
ENST00000438270.2:c.163C>G
|
ENSP00000403439.2:p.His55Asp
|
|
ENST00000466276.2:n.299C>G
|
|
|
ENST00000686129.1:c.163C>G
|
ENSP00000508623.1:p.His55Asp
|
|
ENST00000686523.1:c.*181C>G
|
ENSP00000508940.1:n.*181C>G
|
|
ENST00000687183.1:n.293C>G
|
|
|
ENST00000687198.1:c.163C>G
|
ENSP00000508492.1:p.His55Asp
|
|
ENST00000688117.1:c.331C>G
|
ENSP00000509015.1:p.His111Asp
|
|
ENST00000688244.1:c.232C>G
|
ENSP00000510355.1:p.His78Asp
|
|
ENST00000689001.1:n.639C>G
|
|
|
ENST00000689195.1:c.232C>G
|
ENSP00000509895.1:p.His78Asp
|
|
ENST00000689239.1:n.399C>G
|
|
|
ENST00000689795.1:n.394C>G
|
|
|
ENST00000690835.1:c.232C>G
|
ENSP00000509038.1:p.His78Asp
|
|
ENST00000690993.1:n.309C>G
|
|
|
ENST00000691295.1:c.232C>G
|
ENSP00000508706.1:p.His78Asp
|
|
ENST00000691918.1:c.211C>G
|
ENSP00000509525.1:p.His71Asp
|
|
ENST00000692152.1:c.163C>G
|
ENSP00000509317.1:p.His55Asp
|
|
ENST00000692344.1:n.256C>G
|
|
|
ENST00000693157.1:c.152C>G
|
ENSP00000510610.1:p.Ala51Gly
|
|
ENST00000693363.1:c.232C>G
|
ENSP00000510411.1:p.His78Asp
|
|
ENST00000693367.1:c.232C>G
|
ENSP00000508815.1:p.His78Asp
|
|
ENST00000693639.1:c.225C>G
|
ENSP00000510223.1:p.Ser75Arg
|
|
ENST00000693646.1:c.138C>G
|
ENSP00000508449.1:p.Ser46Arg
|
|
ENST00000693716.1:n.460C>G
|
|
|
ENST00000352397.10:c.232C>G
MANE Select
|
ENSP00000338461.6:p.His78Asp
|
|
ENST00000352397.9:c.232C>G
|
ENSP00000338461.6:p.His78Asp
|
|
ENST00000361740.8:c.331C>G
|
ENSP00000354468.4:p.His111Asp
|
|
ENST00000402438.5:c.163C>G
|
ENSP00000385679.1:p.His55Asp
|
|
ENST00000407332.5:c.163C>G
|
ENSP00000384457.1:p.His55Asp
|
|
ENST00000407623.7:c.163C>G
|
ENSP00000384834.3:p.His55Asp
|
|
ENST00000438270.1:c.163C>G
|
ENSP00000403439.1:p.His55Asp
|
|
ENST00000470741.1:n.2366C>G
|
|
|
NM_000398.6:c.232C>G
|
NP_000389.1:p.His78Asp
|
|
NM_001129819.2:c.163C>G
|
NP_001123291.1:p.His55Asp
|
|
NM_001171660.1:c.331C>G
|
NP_001165131.1:p.His111Asp
|
|
NM_001171661.1:c.163C>G
|
NP_001165132.1:p.His55Asp
|
|
NM_007326.4:c.163C>G
|
NP_015565.1:p.His55Asp
|
|
NM_000398.7:c.232C>G
MANE Select
|
NP_000389.1:p.His78Asp
|
|
NM_001171660.2:c.331C>G
|
NP_001165131.1:p.His111Asp
|
|