ENST00000578493.2:n.706C>T
|
|
|
ENST00000699291.1:c.498C>T
|
ENSP00000514272.1:p.His166=
|
|
ENST00000699292.1:n.413C>T
|
|
|
ENST00000225275.4:c.1373C>T
MANE Select
|
ENSP00000225275.3:p.Thr458Ile
|
|
ENST00000225275.3:c.1373C>T
|
ENSP00000225275.3:p.Thr458Ile
|
|
NM_000250.1:c.1373C>T , LRG_84t1:c.1373C>T
|
NP_000241.1:p.Thr458Ile
|
|
XM_011524821.1:c.1559C>T
|
XP_011523123.1:p.Thr520Ile
|
|
XM_011524822.1:c.1088C>T
|
XP_011523124.1:p.Thr363Ile
|
|
XM_011524823.1:c.1398C>T
|
XP_011523125.1:p.His466=
|
|
NM_000250.2:c.1373C>T
MANE Select
|
NP_000241.1:p.Thr458Ile
|
|