ENST00000578493.2:n.780A>T
|
|
|
ENST00000699291.1:c.572A>T
|
ENSP00000514272.1:p.Gln191Leu
|
|
ENST00000699292.1:n.487A>T
|
|
|
ENST00000225275.4:c.1447A>T
MANE Select
|
ENSP00000225275.3:p.Asn483Tyr
|
|
ENST00000225275.3:c.1447A>T
|
ENSP00000225275.3:p.Asn483Tyr
|
|
NM_000250.1:c.1447A>T , LRG_84t1:c.1447A>T
|
NP_000241.1:p.Asn483Tyr
|
|
XM_011524821.1:c.1633A>T
|
XP_011523123.1:p.Asn545Tyr
|
|
XM_011524822.1:c.1162A>T
|
XP_011523124.1:p.Asn388Tyr
|
|
XM_011524823.1:c.1472A>T
|
XP_011523125.1:p.Gln491Leu
|
|
NM_000250.2:c.1447A>T
MANE Select
|
NP_000241.1:p.Asn483Tyr
|
|