ENST00000394867.9:n.1558G=
|
|
|
ENST00000688002.1:n.3270G=
|
|
|
ENST00000688751.1:n.255G=
|
|
|
ENST00000689792.1:n.1023G=
|
|
|
ENST00000262948.10:c.1119G=
MANE Select
|
ENSP00000262948.4:p.Glu373=
|
|
ENST00000262948.9:c.1119G=
|
ENSP00000262948.3:p.Glu373=
|
|
ENST00000394867.8:c.828G=
|
ENSP00000378336.1:p.Glu276=
|
|
ENST00000597263.5:n.304G=
|
|
|
ENST00000599021.1:c.229G=
|
|
|
ENST00000600584.5:n.2568G=
|
|
|
ENST00000601786.5:n.1420G=
|
|
|
NM_030662.3:c.1119G= , LRG_750t1:c.1119G=
|
NP_109587.1:p.Glu373=
|
|
XM_006722799.2:c.840G=
|
XP_006722862.1:p.Glu280=
|
|
XM_011528133.1:c.549G=
|
XP_011526435.1:p.Glu183=
|
|
NM_030662.4:c.1119G=
MANE Select
|
NP_109587.1:p.Glu373=
|
|