ENST00000578493.2:n.769A>T
|
|
|
ENST00000699291.1:c.561A>T
|
ENSP00000514272.1:p.Val187=
|
|
ENST00000699292.1:n.476A>T
|
|
|
ENST00000225275.4:c.1436A>T
MANE Select
|
ENSP00000225275.3:p.Tyr479Phe
|
|
ENST00000225275.3:c.1436A>T
|
ENSP00000225275.3:p.Tyr479Phe
|
|
NM_000250.1:c.1436A>T , LRG_84t1:c.1436A>T
|
NP_000241.1:p.Tyr479Phe
|
|
XM_011524821.1:c.1622A>T
|
XP_011523123.1:p.Tyr541Phe
|
|
XM_011524822.1:c.1151A>T
|
XP_011523124.1:p.Tyr384Phe
|
|
XM_011524823.1:c.1461A>T
|
XP_011523125.1:p.Val487=
|
|
NM_000250.2:c.1436A>T
MANE Select
|
NP_000241.1:p.Tyr479Phe
|
|