ENST00000371117.8:c.10252G>A
MANE Select
|
ENSP00000360158.3:p.Ala3418Thr
|
|
ENST00000371117.7:c.10252G>A
|
ENSP00000360158.3:p.Ala3418Thr
|
|
NM_138694.3:c.10252G>A
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NP_619639.3:p.Ala3418Thr
|
|
XM_011514679.1:c.10252G>A
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XP_011512981.1:p.Ala3418Thr
|
|
XM_011514680.1:c.10252G>A
|
XP_011512982.1:p.Ala3418Thr
|
|
XM_011514681.1:c.10123G>A
|
XP_011512983.1:p.Ala3375Thr
|
|
XM_011514682.1:c.10114G>A
|
XP_011512984.1:p.Ala3372Thr
|
|
XM_011514683.1:c.9610G>A
|
XP_011512985.1:p.Ala3204Thr
|
|
XM_011514684.1:c.9541G>A
|
XP_011512986.1:p.Ala3181Thr
|
|
XM_011514687.1:c.10157-10654G>A
|
XP_011512989.1:n.10157-10654G>A
|
|
XM_011514690.1:c.4327G>A
|
XP_011512992.1:p.Ala1443Thr
|
|
XM_011514691.1:c.4327G>A
|
XP_011512993.1:p.Ala1443Thr
|
|
XR_926870.1:n.535+7501C>T
|
|
|
XR_926871.1:n.403+7501C>T
|
|
|
XR_926872.1:n.535+7501C>T
|
|
|
XM_011514680.3:c.10252G>A
|
XP_011512982.1:p.Ala3418Thr
|
|
XM_011514682.3:c.10114G>A
|
XP_011512984.1:p.Ala3372Thr
|
|
XM_011514683.3:c.9610G>A
|
XP_011512985.1:p.Ala3204Thr
|
|
XM_011514684.3:c.9541G>A
|
XP_011512986.1:p.Ala3181Thr
|
|
XM_011514690.3:c.4327G>A
|
XP_011512992.1:p.Ala1443Thr
|
|
XM_011514691.3:c.4327G>A
|
XP_011512993.1:p.Ala1443Thr
|
|
XM_017010944.2:c.10252G>A
|
XP_016866433.1:p.Ala3418Thr
|
|
XM_017010945.2:c.10177G>A
|
XP_016866434.1:p.Ala3393Thr
|
|
XM_017010946.2:c.10057G>A
|
XP_016866435.1:p.Ala3353Thr
|
|
XM_017010947.2:c.9988G>A
|
XP_016866436.1:p.Ala3330Thr
|
|
XM_017010948.2:c.9541G>A
|
XP_016866437.1:p.Ala3181Thr
|
|
XM_017010949.2:c.8392G>A
|
XP_016866438.1:p.Ala2798Thr
|
|
XR_001743469.1:n.10528G>A
|
|
|
XR_001744157.1:n.3145+7501C>T
|
|
|
XR_926870.2:n.3145+7501C>T
|
|
|
XR_926871.2:n.3013+7501C>T
|
|
|
XR_926872.2:n.3145+7501C>T
|
|
|
NM_138694.4:c.10252G>A
MANE Select
|
NP_619639.3:p.Ala3418Thr
|
|