ENST00000371117.8:c.10212C>T
MANE Select
|
ENSP00000360158.3:p.Ile3404=
|
|
ENST00000371117.7:c.10212C>T
|
ENSP00000360158.3:p.Ile3404=
|
|
NM_138694.3:c.10212C>T
|
NP_619639.3:p.Ile3404=
|
|
XM_011514679.1:c.10212C>T
|
XP_011512981.1:p.Ile3404=
|
|
XM_011514680.1:c.10212C>T
|
XP_011512982.1:p.Ile3404=
|
|
XM_011514681.1:c.10083C>T
|
XP_011512983.1:p.Ile3361=
|
|
XM_011514682.1:c.10074C>T
|
XP_011512984.1:p.Ile3358=
|
|
XM_011514683.1:c.9570C>T
|
XP_011512985.1:p.Ile3190=
|
|
XM_011514684.1:c.9501C>T
|
XP_011512986.1:p.Ile3167=
|
|
XM_011514687.1:c.10157-10694C>T
|
XP_011512989.1:n.10157-10694C>T
|
|
XM_011514690.1:c.4287C>T
|
XP_011512992.1:p.Ile1429=
|
|
XM_011514691.1:c.4287C>T
|
XP_011512993.1:p.Ile1429=
|
|
XR_926870.1:n.535+7541G>A
|
|
|
XR_926871.1:n.403+7541G>A
|
|
|
XR_926872.1:n.535+7541G>A
|
|
|
XM_011514680.3:c.10212C>T
|
XP_011512982.1:p.Ile3404=
|
|
XM_011514682.3:c.10074C>T
|
XP_011512984.1:p.Ile3358=
|
|
XM_011514683.3:c.9570C>T
|
XP_011512985.1:p.Ile3190=
|
|
XM_011514684.3:c.9501C>T
|
XP_011512986.1:p.Ile3167=
|
|
XM_011514690.3:c.4287C>T
|
XP_011512992.1:p.Ile1429=
|
|
XM_011514691.3:c.4287C>T
|
XP_011512993.1:p.Ile1429=
|
|
XM_017010944.2:c.10212C>T
|
XP_016866433.1:p.Ile3404=
|
|
XM_017010945.2:c.10137C>T
|
XP_016866434.1:p.Ile3379=
|
|
XM_017010946.2:c.10017C>T
|
XP_016866435.1:p.Ile3339=
|
|
XM_017010947.2:c.9948C>T
|
XP_016866436.1:p.Ile3316=
|
|
XM_017010948.2:c.9501C>T
|
XP_016866437.1:p.Ile3167=
|
|
XM_017010949.2:c.8352C>T
|
XP_016866438.1:p.Ile2784=
|
|
XR_001743469.1:n.10488C>T
|
|
|
XR_001744157.1:n.3145+7541G>A
|
|
|
XR_926870.2:n.3145+7541G>A
|
|
|
XR_926871.2:n.3013+7541G>A
|
|
|
XR_926872.2:n.3145+7541G>A
|
|
|
NM_138694.4:c.10212C>T
MANE Select
|
NP_619639.3:p.Ile3404=
|
|