ENST00000270357.10:c.1559A>C
MANE Select
|
ENSP00000270357.4:p.Glu520Ala
|
|
ENST00000270357.8:c.866A>C
|
ENSP00000270357.3:p.Glu289Ala
|
|
ENST00000437406.1:c.125A>C
|
ENSP00000403319.1:p.Glu42Ala
|
|
ENST00000451363.5:c.200A>C
|
ENSP00000414661.1:p.Glu67Ala
|
|
ENST00000464550.5:n.395A>C
|
|
|
ENST00000471657.1:n.362A>C
|
|
|
ENST00000481757.5:n.2493A>C
|
|
|
ENST00000486058.5:n.1672A>C
|
|
|
ENST00000493398.5:n.705A>C
|
|
|
NM_018226.4:c.1559A>C
|
NP_060696.4:p.Glu520Ala
|
|
XM_005247036.3:c.1526A>C
|
XP_005247093.1:p.Glu509Ala
|
|
NM_018226.5:c.1559A>C
|
NP_060696.4:p.Glu520Ala
|
|
XM_005247036.4:c.1526A>C
|
XP_005247093.1:p.Glu509Ala
|
|
NM_018226.6:c.1559A>C
MANE Select
|
NP_060696.4:p.Glu520Ala
|
|