ENST00000270357.10:c.1566C>G
MANE Select
|
ENSP00000270357.4:p.Asp522Glu
|
|
ENST00000270357.8:c.873C>G
|
ENSP00000270357.3:p.Asp291Glu
|
|
ENST00000437406.1:c.132C>G
|
ENSP00000403319.1:p.Asp44Glu
|
|
ENST00000451363.5:c.207C>G
|
ENSP00000414661.1:p.Asp69Glu
|
|
ENST00000464550.5:n.402C>G
|
|
|
ENST00000471657.1:n.369C>G
|
|
|
ENST00000481757.5:n.2500C>G
|
|
|
ENST00000486058.5:n.1679C>G
|
|
|
ENST00000493398.5:n.712C>G
|
|
|
NM_018226.4:c.1566C>G
|
NP_060696.4:p.Asp522Glu
|
|
XM_005247036.3:c.1533C>G
|
XP_005247093.1:p.Asp511Glu
|
|
NM_018226.5:c.1566C>G
|
NP_060696.4:p.Asp522Glu
|
|
XM_005247036.4:c.1533C>G
|
XP_005247093.1:p.Asp511Glu
|
|
NM_018226.6:c.1566C>G
MANE Select
|
NP_060696.4:p.Asp522Glu
|
|