ENST00000270357.10:c.1558G=
MANE Select
|
ENSP00000270357.4:p.Glu520=
|
|
ENST00000270357.8:c.865G=
|
ENSP00000270357.3:p.Glu289=
|
|
ENST00000437406.1:c.124G=
|
ENSP00000403319.1:p.Glu42=
|
|
ENST00000451363.5:c.199G=
|
ENSP00000414661.1:p.Glu67=
|
|
ENST00000464550.5:n.394G=
|
|
|
ENST00000471657.1:n.361G=
|
|
|
ENST00000481757.5:n.2492G=
|
|
|
ENST00000486058.5:n.1671G=
|
|
|
ENST00000493398.5:n.704G=
|
|
|
NM_018226.4:c.1558G=
|
NP_060696.4:p.Glu520=
|
|
XM_005247036.3:c.1525G=
|
XP_005247093.1:p.Glu509=
|
|
NM_018226.5:c.1558G=
|
NP_060696.4:p.Glu520=
|
|
XM_005247036.4:c.1525G=
|
XP_005247093.1:p.Glu509=
|
|
NM_018226.6:c.1558G=
MANE Select
|
NP_060696.4:p.Glu520=
|
|