ENST00000320895.10:c.749G>A
MANE Select
|
ENSP00000313854.5:p.Arg250His
|
|
ENST00000320895.9:c.749G>A
|
ENSP00000313854.5:p.Arg250His
|
|
ENST00000503151.5:n.18G>A
|
|
|
ENST00000507807.3:c.350G>A
|
ENSP00000423321.1:p.Arg117His
|
|
ENST00000508765.5:n.52G>A
|
|
|
ENST00000511786.1:n.486G>A
|
|
|
ENST00000630539.1:c.350G>A
|
ENSP00000485923.1:p.Arg117His
|
|
NM_030782.3:c.749G>A
|
NP_110409.2:p.Arg250His
|
|
NM_030782.4:c.749G>A
|
NP_110409.2:p.Arg250His
|
|
XM_011514144.1:c.746G>A
|
XP_011512446.1:p.Arg249His
|
|
XM_011514144.2:c.746G>A
|
XP_011512446.1:p.Arg249His
|
|
XM_024446221.1:c.749G>A
|
XP_024301989.1:p.Arg250His
|
|
XM_024446222.1:c.215G>A
|
XP_024301990.1:p.Arg72His
|
|
XR_002956182.1:n.792G>A
|
|
|
XR_002956183.1:n.970G>A
|
|
|
NM_030782.5:c.749G>A
MANE Select
|
NP_110409.2:p.Arg250His
|
|