ENST00000557088.6:c.*1129A>C
|
ENSP00000451002.1:n.*1129A>C
|
|
ENST00000557570.2:c.995A>C
|
ENSP00000450787.2:p.Glu332Ala
|
|
ENST00000706675.1:n.978A>C
|
|
|
ENST00000706676.1:c.1337A>C
|
ENSP00000516492.1:p.Glu446Ala
|
|
ENST00000706677.1:c.1163A>C
|
ENSP00000516493.1:p.Glu388Ala
|
|
ENST00000706678.1:n.1083A>C
|
|
|
ENST00000706679.1:c.995A>C
|
ENSP00000516494.1:p.Glu332Ala
|
|
ENST00000706680.1:c.*1006A>C
|
ENSP00000516495.1:n.*1006A>C
|
|
ENST00000706681.1:c.*902A>C
|
ENSP00000516496.1:n.*902A>C
|
|
ENST00000342058.9:c.1163A>C
MANE Select
|
ENSP00000345008.4:p.Glu388Ala
|
|
ENST00000267620.14:c.1286A>C
|
ENSP00000267620.10:p.Glu429Ala
|
|
ENST00000342058.8:c.1163A>C
|
ENSP00000345008.4:p.Glu388Ala
|
|
ENST00000554121.2:n.289A>C
|
|
|
ENST00000556154.5:c.1178A>C
|
ENSP00000451982.1:p.Glu393Ala
|
|
NM_006329.3:c.1163A>C , LRG_364t1:c.1163A>C
|
NP_006320.2:p.Glu388Ala
|
|
XM_005267267.3:c.1214A>C
|
XP_005267324.1:p.Glu405Ala
|
|
XM_011536356.1:c.1214A>C
|
XP_011534658.1:p.Glu405Ala
|
|
XM_011536357.1:c.1163A>C
|
XP_011534659.1:p.Glu388Ala
|
|
XM_011536358.1:c.995A>C
|
XP_011534660.1:p.Glu332Ala
|
|
XM_011536357.2:c.1163A>C
|
XP_011534659.1:p.Glu388Ala
|
|
XM_011536358.2:c.995A>C
|
XP_011534660.1:p.Glu332Ala
|
|
XM_017020929.2:c.995A>C
|
XP_016876418.1:p.Glu332Ala
|
|
NM_001384158.1:c.1286A>C
|
NP_001371087.1:p.Glu429Ala
|
|
NM_001384159.1:c.1214A>C
|
NP_001371088.1:p.Glu405Ala
|
|
NM_001384160.1:c.1163A>C
|
NP_001371089.1:p.Glu388Ala
|
|
NM_001384161.1:c.995A>C
|
NP_001371090.1:p.Glu332Ala
|
|
NM_001384162.1:c.995A>C
|
NP_001371091.1:p.Glu332Ala
|
|
NM_006329.4:c.1163A>C
MANE Select
|
NP_006320.2:p.Glu388Ala
|
|