ENST00000380707.9:c.726A>C
MANE Select
|
ENSP00000370083.4:p.Ile242=
|
|
ENST00000351205.8:c.726A>C
|
ENSP00000305857.5:p.Ile242=
|
|
ENST00000380707.8:c.726A>C
|
ENSP00000370083.4:p.Ile242=
|
|
ENST00000503079.6:c.630A>C
|
ENSP00000428128.1:p.Ile210=
|
|
ENST00000506163.5:c.726A>C
|
ENSP00000424926.1:p.Ile242=
|
|
ENST00000506239.6:c.726A>C
|
ENSP00000422679.2:p.Ile242=
|
|
ENST00000507905.6:c.420A>C
|
ENSP00000430657.1:n.420A>C
|
|
ENST00000513228.1:n.293A>C
|
|
|
ENST00000514951.5:c.525A>C
|
ENSP00000423298.1:p.Ile175=
|
|
ENST00000518504.5:n.243A>C
|
|
|
ENST00000625245.2:c.726A>C
|
ENSP00000486539.1:p.Ile242=
|
|
NM_000344.3:c.726A>C , LRG_676t1:c.726A>C
|
NP_000335.1:p.Ile242=
|
|
NM_001297715.1:c.726A>C
|
NP_001284644.1:p.Ile242=
|
|
NM_022874.2:c.630A>C
|
NP_075012.1:p.Ile210=
|
|
XM_011543596.1:c.726A>C
|
XP_011541898.1:p.Ile242=
|
|
XM_011543597.1:c.525A>C
|
XP_011541899.1:p.Ile175=
|
|
XM_011543598.1:c.429A>C
|
XP_011541900.1:p.Ile143=
|
|
XM_011543598.3:c.429A>C
|
XP_011541900.1:p.Ile143=
|
|
XM_017009786.1:c.630A>C
|
XP_016865275.1:p.Ile210=
|
|
NM_000344.4:c.726A>C
MANE Select
|
NP_000335.1:p.Ile242=
|
|