ENST00000394867.9:n.1617G=
|
|
|
ENST00000688002.1:n.3329G=
|
|
|
ENST00000688751.1:n.314G=
|
|
|
ENST00000689792.1:n.1082G=
|
|
|
ENST00000262948.10:c.1178G=
MANE Select
|
ENSP00000262948.4:p.Gly393=
|
|
ENST00000262948.9:c.1178G=
|
ENSP00000262948.3:p.Gly393=
|
|
ENST00000394867.8:c.887G=
|
ENSP00000378336.1:p.Gly296=
|
|
ENST00000597263.5:n.363G=
|
|
|
ENST00000599021.1:c.288G=
|
|
|
ENST00000600584.5:n.2627G=
|
|
|
ENST00000601786.5:n.1479G=
|
|
|
NM_030662.3:c.1178G= , LRG_750t1:c.1178G=
|
NP_109587.1:p.Gly393=
|
|
XM_006722799.2:c.899G=
|
XP_006722862.1:p.Gly300=
|
|
XM_011528133.1:c.608G=
|
XP_011526435.1:p.Gly203=
|
|
NM_030662.4:c.1178G=
MANE Select
|
NP_109587.1:p.Gly393=
|
|