ENST00000270357.10:c.1577G>T
MANE Select
|
ENSP00000270357.4:p.Gly526Val
|
|
ENST00000270357.8:c.884G>T
|
ENSP00000270357.3:p.Gly295Val
|
|
ENST00000437406.1:c.143G>T
|
ENSP00000403319.1:p.Gly48Val
|
|
ENST00000451363.5:c.218G>T
|
ENSP00000414661.1:p.Gly73Val
|
|
ENST00000464550.5:n.413G>T
|
|
|
ENST00000471657.1:n.380G>T
|
|
|
ENST00000481757.5:n.2511G>T
|
|
|
ENST00000486058.5:n.1690G>T
|
|
|
ENST00000493398.5:n.723G>T
|
|
|
NM_018226.4:c.1577G>T
|
NP_060696.4:p.Gly526Val
|
|
XM_005247036.3:c.1544G>T
|
XP_005247093.1:p.Gly515Val
|
|
NM_018226.5:c.1577G>T
|
NP_060696.4:p.Gly526Val
|
|
XM_005247036.4:c.1544G>T
|
XP_005247093.1:p.Gly515Val
|
|
NM_018226.6:c.1577G>T
MANE Select
|
NP_060696.4:p.Gly526Val
|
|