ENST00000394867.9:n.1504G=
|
|
|
ENST00000688002.1:n.3216G=
|
|
|
ENST00000688751.1:n.201G=
|
|
|
ENST00000689792.1:n.969G=
|
|
|
ENST00000262948.10:c.1065G=
MANE Select
|
ENSP00000262948.4:p.Ala355=
|
|
ENST00000262948.9:c.1065G=
|
ENSP00000262948.3:p.Ala355=
|
|
ENST00000394867.8:c.774G=
|
ENSP00000378336.1:p.Ala258=
|
|
ENST00000597263.5:n.250G=
|
|
|
ENST00000599021.1:c.175G=
|
|
|
ENST00000600584.5:n.2514G=
|
|
|
ENST00000601786.5:n.1366G=
|
|
|
NM_030662.3:c.1065G= , LRG_750t1:c.1065G=
|
NP_109587.1:p.Ala355=
|
|
XM_006722799.2:c.786G=
|
XP_006722862.1:p.Ala262=
|
|
XM_011528133.1:c.495G=
|
XP_011526435.1:p.Ala165=
|
|
NM_030662.4:c.1065G=
MANE Select
|
NP_109587.1:p.Ala355=
|
|