ENST00000578493.2:n.718A>T
|
|
|
ENST00000699291.1:c.510A>T
|
ENSP00000514272.1:p.Leu170=
|
|
ENST00000699292.1:n.425A>T
|
|
|
ENST00000225275.4:c.1385A>T
MANE Select
|
ENSP00000225275.3:p.Tyr462Phe
|
|
ENST00000225275.3:c.1385A>T
|
ENSP00000225275.3:p.Tyr462Phe
|
|
NM_000250.1:c.1385A>T , LRG_84t1:c.1385A>T
|
NP_000241.1:p.Tyr462Phe
|
|
XM_011524821.1:c.1571A>T
|
XP_011523123.1:p.Tyr524Phe
|
|
XM_011524822.1:c.1100A>T
|
XP_011523124.1:p.Tyr367Phe
|
|
XM_011524823.1:c.1410A>T
|
XP_011523125.1:p.Leu470=
|
|
NM_000250.2:c.1385A>T
MANE Select
|
NP_000241.1:p.Tyr462Phe
|
|