ENST00000361740.9:c.771G>T
|
ENSP00000354468.5:p.Glu257Asp
|
|
ENST00000402438.6:c.570G>T
|
ENSP00000385679.1:p.Glu190Asp
|
|
ENST00000407332.6:c.657G>T
|
ENSP00000384457.2:p.Glu219Asp
|
|
ENST00000407623.8:c.570G>T
|
ENSP00000384834.3:p.Glu190Asp
|
|
ENST00000617178.5:c.176G>T
|
|
|
ENST00000684963.1:n.2379G>T
|
|
|
ENST00000685184.1:n.231G>T
|
|
|
ENST00000686523.1:c.*588G>T
|
ENSP00000508940.1:n.*588G>T
|
|
ENST00000687183.1:n.915G>T
|
|
|
ENST00000687198.1:c.570G>T
|
ENSP00000508492.1:p.Glu190Asp
|
|
ENST00000688117.1:c.738G>T
|
ENSP00000509015.1:p.Glu246Asp
|
|
ENST00000688244.1:c.339G>T
|
ENSP00000510355.1:p.Glu113Asp
|
|
ENST00000689001.1:n.1261G>T
|
|
|
ENST00000689195.1:c.555G>T
|
ENSP00000509895.1:p.Glu185Asp
|
|
ENST00000689239.1:n.806G>T
|
|
|
ENST00000689795.1:n.900G>T
|
|
|
ENST00000690835.1:c.*18G>T
|
ENSP00000509038.1:n.*18G>T
|
|
ENST00000690993.1:n.1394G>T
|
|
|
ENST00000691295.1:c.*122G>T
|
ENSP00000508706.1:n.*122G>T
|
|
ENST00000691918.1:c.929G>T
|
ENSP00000509525.1:n.929G>T
|
|
ENST00000692152.1:c.570G>T
|
ENSP00000509317.1:p.Glu190Asp
|
|
ENST00000692344.1:n.1126G>T
|
|
|
ENST00000693363.1:c.681G>T
|
ENSP00000510411.1:p.Glu227Asp
|
|
ENST00000693367.1:c.639G>T
|
ENSP00000508815.1:p.Glu213Asp
|
|
ENST00000693639.1:c.632G>T
|
ENSP00000510223.1:n.632G>T
|
|
ENST00000693646.1:c.545G>T
|
ENSP00000508449.1:n.545G>T
|
|
ENST00000352397.10:c.639G>T
MANE Select
|
ENSP00000338461.6:p.Glu213Asp
|
|
ENST00000352397.9:c.639G>T
|
ENSP00000338461.6:p.Glu213Asp
|
|
ENST00000361740.8:c.738G>T
|
ENSP00000354468.4:p.Glu246Asp
|
|
ENST00000402438.5:c.570G>T
|
ENSP00000385679.1:p.Glu190Asp
|
|
ENST00000407332.5:c.570G>T
|
ENSP00000384457.1:p.Glu190Asp
|
|
ENST00000407623.7:c.570G>T
|
ENSP00000384834.3:p.Glu190Asp
|
|
ENST00000470741.1:n.2773G>T
|
|
|
NM_000398.6:c.639G>T
|
NP_000389.1:p.Glu213Asp
|
|
NM_001129819.2:c.570G>T
|
NP_001123291.1:p.Glu190Asp
|
|
NM_001171660.1:c.738G>T
|
NP_001165131.1:p.Glu246Asp
|
|
NM_001171661.1:c.570G>T
|
NP_001165132.1:p.Glu190Asp
|
|
NM_007326.4:c.570G>T
|
NP_015565.1:p.Glu190Asp
|
|
NM_000398.7:c.639G>T
MANE Select
|
NP_000389.1:p.Glu213Asp
|
|
NM_001171660.2:c.738G>T
|
NP_001165131.1:p.Glu246Asp
|
|