ENST00000578493.2:n.715A>T
|
|
|
ENST00000699291.1:c.507A>T
|
ENSP00000514272.1:p.Gly169=
|
|
ENST00000699292.1:n.422A>T
|
|
|
ENST00000225275.4:c.1382A>T
MANE Select
|
ENSP00000225275.3:p.Asp461Val
|
|
ENST00000225275.3:c.1382A>T
|
ENSP00000225275.3:p.Asp461Val
|
|
NM_000250.1:c.1382A>T , LRG_84t1:c.1382A>T
|
NP_000241.1:p.Asp461Val
|
|
XM_011524821.1:c.1568A>T
|
XP_011523123.1:p.Asp523Val
|
|
XM_011524822.1:c.1097A>T
|
XP_011523124.1:p.Asp366Val
|
|
XM_011524823.1:c.1407A>T
|
XP_011523125.1:p.Gly469=
|
|
NM_000250.2:c.1382A>T
MANE Select
|
NP_000241.1:p.Asp461Val
|
|