ENST00000251654.9:c.862G=
MANE Select
|
ENSP00000251654.4:p.Val288=
|
|
ENST00000251654.8:c.862G=
|
ENSP00000251654.4:p.Val288=
|
|
ENST00000462637.5:c.793G=
|
ENSP00000420391.1:p.Val265=
|
|
ENST00000466072.5:c.862G=
|
ENSP00000420158.1:p.Val288=
|
|
ENST00000468777.5:c.955G=
|
ENSP00000419129.1:p.Val319=
|
|
ENST00000469217.5:c.922G=
|
ENSP00000419027.1:p.Val308=
|
|
ENST00000471595.5:c.862G=
|
ENSP00000417549.1:p.Val288=
|
|
ENST00000473073.1:n.819G=
|
|
|
ENST00000474833.5:n.487G=
|
|
|
ENST00000475214.5:n.776G=
|
|
|
ENST00000478469.5:c.862G=
|
ENSP00000420759.1:p.Val288=
|
|
ENST00000482086.5:c.514G=
|
ENSP00000417253.1:p.Val172=
|
|
ENST00000483687.5:c.805G=
|
ENSP00000420639.1:p.Val269=
|
|
ENST00000484181.5:c.862G=
|
ENSP00000417937.1:p.Val288=
|
|
ENST00000490504.5:c.691G=
|
ENSP00000418307.1:p.Val231=
|
|
NM_000532.4:c.862G=
|
NP_000523.2:p.Val288=
|
|
NM_001178014.1:c.922G=
|
NP_001171485.1:p.Val308=
|
|
XM_011512873.1:c.862G=
|
XP_011511175.1:p.Val288=
|
|
XM_011512873.2:c.862G=
|
XP_011511175.1:p.Val288=
|
|
NM_000532.5:c.862G=
MANE Select
|
NP_000523.2:p.Val288=
|
|
NM_001178014.2:c.922G=
|
NP_001171485.1:p.Val308=
|
|