ENST00000265724.8:c.3250G=
|
ENSP00000265724.3:p.Glu1084=
|
|
ENST00000622132.5:c.3250G=
MANE Select
|
ENSP00000478255.1:p.Glu1084=
|
|
ENST00000265724.7:c.3250G=
|
ENSP00000265724.3:p.Glu1084=
|
|
ENST00000475929.5:n.406G=
|
|
|
ENST00000488737.6:n.892G=
|
|
|
ENST00000496821.5:n.878G=
|
|
|
ENST00000543898.5:c.3058G=
|
ENSP00000444095.1:p.Glu1020=
|
|
ENST00000622132.4:c.3250G=
|
ENSP00000478255.1:p.Glu1084=
|
|
NM_000927.4:c.3250G=
|
NP_000918.2:p.Glu1084=
|
|
NM_001348944.1:c.3250G=
|
NP_001335873.1:p.Glu1084=
|
|
NM_001348945.1:c.3460G=
|
NP_001335874.1:p.Glu1154=
|
|
NM_001348946.1:c.3250G=
|
NP_001335875.1:p.Glu1084=
|
|
NM_001348946.2:c.3250G=
MANE Select
|
NP_001335875.1:p.Glu1084=
|
|
NM_000927.5:c.3250G=
|
NP_000918.2:p.Glu1084=
|
|
NM_001348944.2:c.3250G=
|
NP_001335873.1:p.Glu1084=
|
|
NM_001348945.2:c.3460G=
|
NP_001335874.1:p.Glu1154=
|
|