ENST00000361740.9:c.793G>T
|
ENSP00000354468.5:p.Glu265Ter
|
|
ENST00000402438.6:c.592G>T
|
ENSP00000385679.1:p.Glu198Ter
|
|
ENST00000407332.6:c.679G>T
|
ENSP00000384457.2:p.Glu227Ter
|
|
ENST00000407623.8:c.592G>T
|
ENSP00000384834.3:p.Glu198Ter
|
|
ENST00000617178.5:c.198G>T
|
|
|
ENST00000684963.1:n.2401G>T
|
|
|
ENST00000685184.1:n.253G>T
|
|
|
ENST00000686523.1:c.*610G>T
|
ENSP00000508940.1:n.*610G>T
|
|
ENST00000687183.1:n.937G>T
|
|
|
ENST00000687198.1:c.592G>T
|
ENSP00000508492.1:p.Glu198Ter
|
|
ENST00000688117.1:c.760G>T
|
ENSP00000509015.1:p.Glu254Ter
|
|
ENST00000688244.1:c.361G>T
|
ENSP00000510355.1:p.Glu121Ter
|
|
ENST00000689001.1:n.1283G>T
|
|
|
ENST00000689195.1:c.577G>T
|
ENSP00000509895.1:p.Glu193Ter
|
|
ENST00000689239.1:n.828G>T
|
|
|
ENST00000689795.1:n.922G>T
|
|
|
ENST00000690835.1:c.*40G>T
|
ENSP00000509038.1:n.*40G>T
|
|
ENST00000690993.1:n.1416G>T
|
|
|
ENST00000691295.1:c.*144G>T
|
ENSP00000508706.1:n.*144G>T
|
|
ENST00000691918.1:c.951G>T
|
ENSP00000509525.1:n.951G>T
|
|
ENST00000692152.1:c.592G>T
|
ENSP00000509317.1:p.Glu198Ter
|
|
ENST00000692344.1:n.1148G>T
|
|
|
ENST00000693363.1:c.703G>T
|
ENSP00000510411.1:p.Glu235Ter
|
|
ENST00000693367.1:c.661G>T
|
ENSP00000508815.1:p.Glu221Ter
|
|
ENST00000693639.1:c.654G>T
|
ENSP00000510223.1:n.654G>T
|
|
ENST00000693646.1:c.567G>T
|
ENSP00000508449.1:n.567G>T
|
|
ENST00000352397.10:c.661G>T
MANE Select
|
ENSP00000338461.6:p.Glu221Ter
|
|
ENST00000352397.9:c.661G>T
|
ENSP00000338461.6:p.Glu221Ter
|
|
ENST00000361740.8:c.760G>T
|
ENSP00000354468.4:p.Glu254Ter
|
|
ENST00000402438.5:c.592G>T
|
ENSP00000385679.1:p.Glu198Ter
|
|
ENST00000407332.5:c.592G>T
|
ENSP00000384457.1:p.Glu198Ter
|
|
ENST00000407623.7:c.592G>T
|
ENSP00000384834.3:p.Glu198Ter
|
|
ENST00000470741.1:n.2795G>T
|
|
|
NM_000398.6:c.661G>T
|
NP_000389.1:p.Glu221Ter
|
|
NM_001129819.2:c.592G>T
|
NP_001123291.1:p.Glu198Ter
|
|
NM_001171660.1:c.760G>T
|
NP_001165131.1:p.Glu254Ter
|
|
NM_001171661.1:c.592G>T
|
NP_001165132.1:p.Glu198Ter
|
|
NM_007326.4:c.592G>T
|
NP_015565.1:p.Glu198Ter
|
|
NM_000398.7:c.661G>T
MANE Select
|
NP_000389.1:p.Glu221Ter
|
|
NM_001171660.2:c.760G>T
|
NP_001165131.1:p.Glu254Ter
|
|