ENST00000361740.9:c.743G>A
|
ENSP00000354468.5:p.Cys248Tyr
|
|
ENST00000402438.6:c.542G>A
|
ENSP00000385679.1:p.Cys181Tyr
|
|
ENST00000407332.6:c.629G>A
|
ENSP00000384457.2:p.Cys210Tyr
|
|
ENST00000407623.8:c.542G>A
|
ENSP00000384834.3:p.Cys181Tyr
|
|
ENST00000617178.5:c.148G>A
|
|
|
ENST00000684963.1:n.2351G>A
|
|
|
ENST00000686523.1:c.*560G>A
|
ENSP00000508940.1:n.*560G>A
|
|
ENST00000687183.1:n.887G>A
|
|
|
ENST00000687198.1:c.542G>A
|
ENSP00000508492.1:p.Cys181Tyr
|
|
ENST00000688117.1:c.710G>A
|
ENSP00000509015.1:p.Cys237Tyr
|
|
ENST00000688244.1:c.334-3438G>A
|
ENSP00000510355.1:n.334-3438G>A
|
|
ENST00000689001.1:n.1233G>A
|
|
|
ENST00000689195.1:c.527G>A
|
ENSP00000509895.1:p.Cys176Tyr
|
|
ENST00000689239.1:n.778G>A
|
|
|
ENST00000689795.1:n.773G>A
|
|
|
ENST00000690835.1:c.611G>A
|
ENSP00000509038.1:p.Cys204Tyr
|
|
ENST00000690993.1:n.1366G>A
|
|
|
ENST00000691295.1:c.*94G>A
|
ENSP00000508706.1:n.*94G>A
|
|
ENST00000691918.1:c.590G>A
|
ENSP00000509525.1:p.Cys197Tyr
|
|
ENST00000692152.1:c.542G>A
|
ENSP00000509317.1:p.Cys181Tyr
|
|
ENST00000692344.1:n.1098G>A
|
|
|
ENST00000693363.1:c.653G>A
|
ENSP00000510411.1:p.Cys218Tyr
|
|
ENST00000693367.1:c.611G>A
|
ENSP00000508815.1:p.Cys204Tyr
|
|
ENST00000693639.1:c.604G>A
|
ENSP00000510223.1:n.604G>A
|
|
ENST00000693646.1:c.517G>A
|
ENSP00000508449.1:n.517G>A
|
|
ENST00000352397.10:c.611G>A
MANE Select
|
ENSP00000338461.6:p.Cys204Tyr
|
|
ENST00000352397.9:c.611G>A
|
ENSP00000338461.6:p.Cys204Tyr
|
|
ENST00000361740.8:c.710G>A
|
ENSP00000354468.4:p.Cys237Tyr
|
|
ENST00000402438.5:c.542G>A
|
ENSP00000385679.1:p.Cys181Tyr
|
|
ENST00000407332.5:c.542G>A
|
ENSP00000384457.1:p.Cys181Tyr
|
|
ENST00000407623.7:c.542G>A
|
ENSP00000384834.3:p.Cys181Tyr
|
|
ENST00000470741.1:n.2745G>A
|
|
|
NM_000398.6:c.611G>A
|
NP_000389.1:p.Cys204Tyr
|
|
NM_001129819.2:c.542G>A
|
NP_001123291.1:p.Cys181Tyr
|
|
NM_001171660.1:c.710G>A
|
NP_001165131.1:p.Cys237Tyr
|
|
NM_001171661.1:c.542G>A
|
NP_001165132.1:p.Cys181Tyr
|
|
NM_007326.4:c.542G>A
|
NP_015565.1:p.Cys181Tyr
|
|
NM_000398.7:c.611G>A
MANE Select
|
NP_000389.1:p.Cys204Tyr
|
|
NM_001171660.2:c.710G>A
|
NP_001165131.1:p.Cys237Tyr
|
|