ENST00000270357.10:c.1564G>C
MANE Select
|
ENSP00000270357.4:p.Asp522His
|
|
ENST00000270357.8:c.871G>C
|
ENSP00000270357.3:p.Asp291His
|
|
ENST00000437406.1:c.130G>C
|
ENSP00000403319.1:p.Asp44His
|
|
ENST00000451363.5:c.205G>C
|
ENSP00000414661.1:p.Asp69His
|
|
ENST00000464550.5:n.400G>C
|
|
|
ENST00000471657.1:n.367G>C
|
|
|
ENST00000481757.5:n.2498G>C
|
|
|
ENST00000486058.5:n.1677G>C
|
|
|
ENST00000493398.5:n.710G>C
|
|
|
NM_018226.4:c.1564G>C
|
NP_060696.4:p.Asp522His
|
|
XM_005247036.3:c.1531G>C
|
XP_005247093.1:p.Asp511His
|
|
NM_018226.5:c.1564G>C
|
NP_060696.4:p.Asp522His
|
|
XM_005247036.4:c.1531G>C
|
XP_005247093.1:p.Asp511His
|
|
NM_018226.6:c.1564G>C
MANE Select
|
NP_060696.4:p.Asp522His
|
|