ENST00000361740.9:c.796C>A
|
ENSP00000354468.5:p.Leu266Met
|
|
ENST00000402438.6:c.595C>A
|
ENSP00000385679.1:p.Leu199Met
|
|
ENST00000407332.6:c.682C>A
|
ENSP00000384457.2:p.Leu228Met
|
|
ENST00000407623.8:c.595C>A
|
ENSP00000384834.3:p.Leu199Met
|
|
ENST00000617178.5:c.201C>A
|
|
|
ENST00000684963.1:n.2404C>A
|
|
|
ENST00000685184.1:n.256C>A
|
|
|
ENST00000686523.1:c.*613C>A
|
ENSP00000508940.1:n.*613C>A
|
|
ENST00000687183.1:n.940C>A
|
|
|
ENST00000687198.1:c.595C>A
|
ENSP00000508492.1:p.Leu199Met
|
|
ENST00000688117.1:c.763C>A
|
ENSP00000509015.1:p.Leu255Met
|
|
ENST00000688244.1:c.364C>A
|
ENSP00000510355.1:p.Leu122Met
|
|
ENST00000689001.1:n.1286C>A
|
|
|
ENST00000689195.1:c.580C>A
|
ENSP00000509895.1:p.Leu194Met
|
|
ENST00000689239.1:n.831C>A
|
|
|
ENST00000689795.1:n.925C>A
|
|
|
ENST00000690835.1:c.*43C>A
|
ENSP00000509038.1:n.*43C>A
|
|
ENST00000690993.1:n.1419C>A
|
|
|
ENST00000691295.1:c.*147C>A
|
ENSP00000508706.1:n.*147C>A
|
|
ENST00000691918.1:c.954C>A
|
ENSP00000509525.1:n.954C>A
|
|
ENST00000692152.1:c.595C>A
|
ENSP00000509317.1:p.Leu199Met
|
|
ENST00000692344.1:n.1151C>A
|
|
|
ENST00000693363.1:c.706C>A
|
ENSP00000510411.1:p.Leu236Met
|
|
ENST00000693367.1:c.664C>A
|
ENSP00000508815.1:p.Leu222Met
|
|
ENST00000693639.1:c.657C>A
|
ENSP00000510223.1:n.657C>A
|
|
ENST00000693646.1:c.570C>A
|
ENSP00000508449.1:n.570C>A
|
|
ENST00000352397.10:c.664C>A
MANE Select
|
ENSP00000338461.6:p.Leu222Met
|
|
ENST00000352397.9:c.664C>A
|
ENSP00000338461.6:p.Leu222Met
|
|
ENST00000361740.8:c.763C>A
|
ENSP00000354468.4:p.Leu255Met
|
|
ENST00000402438.5:c.595C>A
|
ENSP00000385679.1:p.Leu199Met
|
|
ENST00000407332.5:c.595C>A
|
ENSP00000384457.1:p.Leu199Met
|
|
ENST00000407623.7:c.595C>A
|
ENSP00000384834.3:p.Leu199Met
|
|
ENST00000470741.1:n.2798C>A
|
|
|
NM_000398.6:c.664C>A
|
NP_000389.1:p.Leu222Met
|
|
NM_001129819.2:c.595C>A
|
NP_001123291.1:p.Leu199Met
|
|
NM_001171660.1:c.763C>A
|
NP_001165131.1:p.Leu255Met
|
|
NM_001171661.1:c.595C>A
|
NP_001165132.1:p.Leu199Met
|
|
NM_007326.4:c.595C>A
|
NP_015565.1:p.Leu199Met
|
|
NM_000398.7:c.664C>A
MANE Select
|
NP_000389.1:p.Leu222Met
|
|
NM_001171660.2:c.763C>A
|
NP_001165131.1:p.Leu255Met
|
|