ENST00000682275.1:c.485A>T
|
ENSP00000507852.1:p.Glu162Val
|
|
ENST00000683395.1:c.475A>T
|
|
|
ENST00000684087.1:c.485A>T
|
ENSP00000506978.1:p.Glu162Val
|
|
ENST00000684700.1:c.485A>T
|
ENSP00000507806.1:p.Glu162Val
|
|
ENST00000506362.2:c.236A>T
|
ENSP00000424103.2:p.Glu79Val
|
|
ENST00000673642.1:c.284A>T
|
ENSP00000501242.1:p.Glu95Val
|
|
ENST00000673991.1:c.485A>T
|
ENSP00000501033.1:p.Glu162Val
|
|
ENST00000674051.1:c.359A>T
|
ENSP00000501083.1:p.Glu120Val
|
|
ENST00000226760.5:c.485A>T
MANE Select
|
ENSP00000226760.1:p.Glu162Val
|
|
ENST00000503569.5:c.485A>T
|
ENSP00000423337.1:p.Glu162Val
|
|
ENST00000506362.1:c.82A>T
|
|
|
ENST00000507765.1:n.670A>T
|
|
|
NM_001145853.1:c.485A>T
|
NP_001139325.1:p.Glu162Val
|
|
NM_006005.3:c.485A>T
MANE Select
|
NP_005996.2:p.Glu162Val
|
|
XM_017008586.1:c.494A>T
|
XP_016864075.1:p.Glu165Val
|
|