ENST00000270357.10:c.1523A>T
MANE Select
|
ENSP00000270357.4:p.Glu508Val
|
|
ENST00000270357.8:c.830A>T
|
ENSP00000270357.3:p.Glu277Val
|
|
ENST00000437406.1:c.110-21A>T
|
ENSP00000403319.1:n.110-21A>T
|
|
ENST00000451363.5:c.164A>T
|
ENSP00000414661.1:p.Glu55Val
|
|
ENST00000464550.5:n.359A>T
|
|
|
ENST00000471657.1:n.326A>T
|
|
|
ENST00000481757.5:n.2457A>T
|
|
|
ENST00000486058.5:n.1636A>T
|
|
|
ENST00000493398.5:n.669A>T
|
|
|
NM_018226.4:c.1523A>T
|
NP_060696.4:p.Glu508Val
|
|
XM_005247036.3:c.1511-21A>T
|
XP_005247093.1:n.1511-21A>T
|
|
NM_018226.5:c.1523A>T
|
NP_060696.4:p.Glu508Val
|
|
XM_005247036.4:c.1511-21A>T
|
XP_005247093.1:n.1511-21A>T
|
|
NM_018226.6:c.1523A>T
MANE Select
|
NP_060696.4:p.Glu508Val
|
|