ENST00000251654.9:c.1534C>A
MANE Select
|
ENSP00000251654.4:p.Arg512Ser
|
|
ENST00000251654.8:c.1534C>A
|
ENSP00000251654.4:p.Arg512Ser
|
|
ENST00000462637.5:c.1465C>A
|
ENSP00000420391.1:p.Arg489Ser
|
|
ENST00000466072.5:c.1594C>A
|
ENSP00000420158.1:p.Arg532Ser
|
|
ENST00000468777.5:c.1627C>A
|
ENSP00000419129.1:p.Arg543Ser
|
|
ENST00000469217.5:c.1594C>A
|
ENSP00000419027.1:p.Arg532Ser
|
|
ENST00000471595.5:c.1534C>A
|
ENSP00000417549.1:p.Arg512Ser
|
|
ENST00000473073.1:n.1735C>A
|
|
|
ENST00000478469.5:c.885-4340C>A
|
ENSP00000420759.1:n.885-4340C>A
|
|
ENST00000482086.5:c.1186C>A
|
ENSP00000417253.1:p.Arg396Ser
|
|
ENST00000483687.5:c.1477C>A
|
ENSP00000420639.1:p.Arg493Ser
|
|
ENST00000484181.5:c.*215C>A
|
ENSP00000417937.1:n.*215C>A
|
|
ENST00000490504.5:c.1363C>A
|
ENSP00000418307.1:p.Arg455Ser
|
|
NM_000532.4:c.1534C>A
|
NP_000523.2:p.Arg512Ser
|
|
NM_001178014.1:c.1594C>A
|
NP_001171485.1:p.Arg532Ser
|
|
NM_000532.5:c.1534C>A
MANE Select
|
NP_000523.2:p.Arg512Ser
|
|
NM_001178014.2:c.1594C>A
|
NP_001171485.1:p.Arg532Ser
|
|