ENST00000251654.9:c.505G=
MANE Select
|
ENSP00000251654.4:p.Gly169=
|
|
ENST00000251654.8:c.505G=
|
ENSP00000251654.4:p.Gly169=
|
|
ENST00000459873.1:c.256G=
|
ENSP00000419293.1:p.Gly86=
|
|
ENST00000462542.5:c.372G=
|
|
|
ENST00000462637.5:c.436G=
|
ENSP00000420391.1:p.Gly146=
|
|
ENST00000465176.5:n.467G=
|
|
|
ENST00000466072.5:c.505G=
|
ENSP00000420158.1:p.Gly169=
|
|
ENST00000468777.5:c.598G=
|
ENSP00000419129.1:p.Gly200=
|
|
ENST00000469217.5:c.565G=
|
ENSP00000419027.1:p.Gly189=
|
|
ENST00000471595.5:c.505G=
|
ENSP00000417549.1:p.Gly169=
|
|
ENST00000473073.1:n.462G=
|
|
|
ENST00000474833.5:n.168+11469G=
|
|
|
ENST00000475214.5:n.419G=
|
|
|
ENST00000478469.5:c.505G=
|
ENSP00000420759.1:p.Gly169=
|
|
ENST00000482086.5:c.157G=
|
ENSP00000417253.1:p.Gly53=
|
|
ENST00000483687.5:c.448G=
|
ENSP00000420639.1:p.Gly150=
|
|
ENST00000484181.5:c.505G=
|
ENSP00000417937.1:p.Gly169=
|
|
ENST00000490504.5:c.372+5404G=
|
ENSP00000418307.1:n.372+5404G=
|
|
NM_000532.4:c.505G=
|
NP_000523.2:p.Gly169=
|
|
NM_001178014.1:c.565G=
|
NP_001171485.1:p.Gly189=
|
|
XM_011512873.1:c.505G=
|
XP_011511175.1:p.Gly169=
|
|
XM_011512873.2:c.505G=
|
XP_011511175.1:p.Gly169=
|
|
NM_000532.5:c.505G=
MANE Select
|
NP_000523.2:p.Gly169=
|
|
NM_001178014.2:c.565G=
|
NP_001171485.1:p.Gly189=
|
|