ENST00000251654.9:c.1203A>T
MANE Select
|
ENSP00000251654.4:p.Thr401=
|
|
ENST00000251654.8:c.1203A>T
|
ENSP00000251654.4:p.Thr401=
|
|
ENST00000462637.5:c.1134A>T
|
ENSP00000420391.1:p.Thr378=
|
|
ENST00000466072.5:c.1263A>T
|
ENSP00000420158.1:p.Thr421=
|
|
ENST00000468777.5:c.1296A>T
|
ENSP00000419129.1:p.Thr432=
|
|
ENST00000469217.5:c.1263A>T
|
ENSP00000419027.1:p.Thr421=
|
|
ENST00000471595.5:c.1203A>T
|
ENSP00000417549.1:p.Thr401=
|
|
ENST00000473073.1:n.1404A>T
|
|
|
ENST00000474833.5:n.823+249A>T
|
|
|
ENST00000478469.5:c.885-7121A>T
|
ENSP00000420759.1:n.885-7121A>T
|
|
ENST00000482086.5:c.855A>T
|
ENSP00000417253.1:p.Thr285=
|
|
ENST00000483687.5:c.1146A>T
|
ENSP00000420639.1:p.Thr382=
|
|
ENST00000484181.5:c.1198+249A>T
|
ENSP00000417937.1:n.1198+249A>T
|
|
ENST00000490504.5:c.1032A>T
|
ENSP00000418307.1:p.Thr344=
|
|
NM_000532.4:c.1203A>T
|
NP_000523.2:p.Thr401=
|
|
NM_001178014.1:c.1263A>T
|
NP_001171485.1:p.Thr421=
|
|
NM_000532.5:c.1203A>T
MANE Select
|
NP_000523.2:p.Thr401=
|
|
NM_001178014.2:c.1263A>T
|
NP_001171485.1:p.Thr421=
|
|