ENST00000361740.9:c.769G>C
|
ENSP00000354468.5:p.Glu257Gln
|
|
ENST00000402438.6:c.568G>C
|
ENSP00000385679.1:p.Glu190Gln
|
|
ENST00000407332.6:c.655G>C
|
ENSP00000384457.2:p.Glu219Gln
|
|
ENST00000407623.8:c.568G>C
|
ENSP00000384834.3:p.Glu190Gln
|
|
ENST00000617178.5:c.174G>C
|
|
|
ENST00000684963.1:n.2377G>C
|
|
|
ENST00000685184.1:n.229G>C
|
|
|
ENST00000686523.1:c.*586G>C
|
ENSP00000508940.1:n.*586G>C
|
|
ENST00000687183.1:n.913G>C
|
|
|
ENST00000687198.1:c.568G>C
|
ENSP00000508492.1:p.Glu190Gln
|
|
ENST00000688117.1:c.736G>C
|
ENSP00000509015.1:p.Glu246Gln
|
|
ENST00000688244.1:c.337G>C
|
ENSP00000510355.1:p.Glu113Gln
|
|
ENST00000689001.1:n.1259G>C
|
|
|
ENST00000689195.1:c.553G>C
|
ENSP00000509895.1:p.Glu185Gln
|
|
ENST00000689239.1:n.804G>C
|
|
|
ENST00000689795.1:n.898G>C
|
|
|
ENST00000690835.1:c.*16G>C
|
ENSP00000509038.1:n.*16G>C
|
|
ENST00000690993.1:n.1392G>C
|
|
|
ENST00000691295.1:c.*120G>C
|
ENSP00000508706.1:n.*120G>C
|
|
ENST00000691918.1:c.927G>C
|
ENSP00000509525.1:n.927G>C
|
|
ENST00000692152.1:c.568G>C
|
ENSP00000509317.1:p.Glu190Gln
|
|
ENST00000692344.1:n.1124G>C
|
|
|
ENST00000693363.1:c.679G>C
|
ENSP00000510411.1:p.Glu227Gln
|
|
ENST00000693367.1:c.637G>C
|
ENSP00000508815.1:p.Glu213Gln
|
|
ENST00000693639.1:c.630G>C
|
ENSP00000510223.1:n.630G>C
|
|
ENST00000693646.1:c.543G>C
|
ENSP00000508449.1:n.543G>C
|
|
ENST00000352397.10:c.637G>C
MANE Select
|
ENSP00000338461.6:p.Glu213Gln
|
|
ENST00000352397.9:c.637G>C
|
ENSP00000338461.6:p.Glu213Gln
|
|
ENST00000361740.8:c.736G>C
|
ENSP00000354468.4:p.Glu246Gln
|
|
ENST00000402438.5:c.568G>C
|
ENSP00000385679.1:p.Glu190Gln
|
|
ENST00000407332.5:c.568G>C
|
ENSP00000384457.1:p.Glu190Gln
|
|
ENST00000407623.7:c.568G>C
|
ENSP00000384834.3:p.Glu190Gln
|
|
ENST00000470741.1:n.2771G>C
|
|
|
NM_000398.6:c.637G>C
|
NP_000389.1:p.Glu213Gln
|
|
NM_001129819.2:c.568G>C
|
NP_001123291.1:p.Glu190Gln
|
|
NM_001171660.1:c.736G>C
|
NP_001165131.1:p.Glu246Gln
|
|
NM_001171661.1:c.568G>C
|
NP_001165132.1:p.Glu190Gln
|
|
NM_007326.4:c.568G>C
|
NP_015565.1:p.Glu190Gln
|
|
NM_000398.7:c.637G>C
MANE Select
|
NP_000389.1:p.Glu213Gln
|
|
NM_001171660.2:c.736G>C
|
NP_001165131.1:p.Glu246Gln
|
|