ENST00000578493.2:n.714G>T
|
|
|
ENST00000699291.1:c.506G>T
|
ENSP00000514272.1:p.Gly169Val
|
|
ENST00000699292.1:n.421G>T
|
|
|
ENST00000225275.4:c.1381G>T
MANE Select
|
ENSP00000225275.3:p.Asp461Tyr
|
|
ENST00000225275.3:c.1381G>T
|
ENSP00000225275.3:p.Asp461Tyr
|
|
NM_000250.1:c.1381G>T , LRG_84t1:c.1381G>T
|
NP_000241.1:p.Asp461Tyr
|
|
XM_011524821.1:c.1567G>T
|
XP_011523123.1:p.Asp523Tyr
|
|
XM_011524822.1:c.1096G>T
|
XP_011523124.1:p.Asp366Tyr
|
|
XM_011524823.1:c.1406G>T
|
XP_011523125.1:p.Gly469Val
|
|
NM_000250.2:c.1381G>T
MANE Select
|
NP_000241.1:p.Asp461Tyr
|
|