ENST00000270357.10:c.1560G>T
MANE Select
|
ENSP00000270357.4:p.Glu520Asp
|
|
ENST00000270357.8:c.867G>T
|
ENSP00000270357.3:p.Glu289Asp
|
|
ENST00000437406.1:c.126G>T
|
ENSP00000403319.1:p.Glu42Asp
|
|
ENST00000451363.5:c.201G>T
|
ENSP00000414661.1:p.Glu67Asp
|
|
ENST00000464550.5:n.396G>T
|
|
|
ENST00000471657.1:n.363G>T
|
|
|
ENST00000481757.5:n.2494G>T
|
|
|
ENST00000486058.5:n.1673G>T
|
|
|
ENST00000493398.5:n.706G>T
|
|
|
NM_018226.4:c.1560G>T
|
NP_060696.4:p.Glu520Asp
|
|
XM_005247036.3:c.1527G>T
|
XP_005247093.1:p.Glu509Asp
|
|
NM_018226.5:c.1560G>T
|
NP_060696.4:p.Glu520Asp
|
|
XM_005247036.4:c.1527G>T
|
XP_005247093.1:p.Glu509Asp
|
|
NM_018226.6:c.1560G>T
MANE Select
|
NP_060696.4:p.Glu520Asp
|
|