ENST00000270357.10:c.1564G>T
MANE Select
|
ENSP00000270357.4:p.Asp522Tyr
|
|
ENST00000270357.8:c.871G>T
|
ENSP00000270357.3:p.Asp291Tyr
|
|
ENST00000437406.1:c.130G>T
|
ENSP00000403319.1:p.Asp44Tyr
|
|
ENST00000451363.5:c.205G>T
|
ENSP00000414661.1:p.Asp69Tyr
|
|
ENST00000464550.5:n.400G>T
|
|
|
ENST00000471657.1:n.367G>T
|
|
|
ENST00000481757.5:n.2498G>T
|
|
|
ENST00000486058.5:n.1677G>T
|
|
|
ENST00000493398.5:n.710G>T
|
|
|
NM_018226.4:c.1564G>T
|
NP_060696.4:p.Asp522Tyr
|
|
XM_005247036.3:c.1531G>T
|
XP_005247093.1:p.Asp511Tyr
|
|
NM_018226.5:c.1564G>T
|
NP_060696.4:p.Asp522Tyr
|
|
XM_005247036.4:c.1531G>T
|
XP_005247093.1:p.Asp511Tyr
|
|
NM_018226.6:c.1564G>T
MANE Select
|
NP_060696.4:p.Asp522Tyr
|
|