ENST00000371117.8:c.10253C>T
MANE Select
|
ENSP00000360158.3:p.Ala3418Val
|
|
ENST00000371117.7:c.10253C>T
|
ENSP00000360158.3:p.Ala3418Val
|
|
NM_138694.3:c.10253C>T
|
NP_619639.3:p.Ala3418Val
|
|
XM_011514679.1:c.10253C>T
|
XP_011512981.1:p.Ala3418Val
|
|
XM_011514680.1:c.10253C>T
|
XP_011512982.1:p.Ala3418Val
|
|
XM_011514681.1:c.10124C>T
|
XP_011512983.1:p.Ala3375Val
|
|
XM_011514682.1:c.10115C>T
|
XP_011512984.1:p.Ala3372Val
|
|
XM_011514683.1:c.9611C>T
|
XP_011512985.1:p.Ala3204Val
|
|
XM_011514684.1:c.9542C>T
|
XP_011512986.1:p.Ala3181Val
|
|
XM_011514687.1:c.10157-10653C>T
|
XP_011512989.1:n.10157-10653C>T
|
|
XM_011514690.1:c.4328C>T
|
XP_011512992.1:p.Ala1443Val
|
|
XM_011514691.1:c.4328C>T
|
XP_011512993.1:p.Ala1443Val
|
|
XR_926870.1:n.535+7500G>A
|
|
|
XR_926871.1:n.403+7500G>A
|
|
|
XR_926872.1:n.535+7500G>A
|
|
|
XM_011514680.3:c.10253C>T
|
XP_011512982.1:p.Ala3418Val
|
|
XM_011514682.3:c.10115C>T
|
XP_011512984.1:p.Ala3372Val
|
|
XM_011514683.3:c.9611C>T
|
XP_011512985.1:p.Ala3204Val
|
|
XM_011514684.3:c.9542C>T
|
XP_011512986.1:p.Ala3181Val
|
|
XM_011514690.3:c.4328C>T
|
XP_011512992.1:p.Ala1443Val
|
|
XM_011514691.3:c.4328C>T
|
XP_011512993.1:p.Ala1443Val
|
|
XM_017010944.2:c.10253C>T
|
XP_016866433.1:p.Ala3418Val
|
|
XM_017010945.2:c.10178C>T
|
XP_016866434.1:p.Ala3393Val
|
|
XM_017010946.2:c.10058C>T
|
XP_016866435.1:p.Ala3353Val
|
|
XM_017010947.2:c.9989C>T
|
XP_016866436.1:p.Ala3330Val
|
|
XM_017010948.2:c.9542C>T
|
XP_016866437.1:p.Ala3181Val
|
|
XM_017010949.2:c.8393C>T
|
XP_016866438.1:p.Ala2798Val
|
|
XR_001743469.1:n.10529C>T
|
|
|
XR_001744157.1:n.3145+7500G>A
|
|
|
XR_926870.2:n.3145+7500G>A
|
|
|
XR_926871.2:n.3013+7500G>A
|
|
|
XR_926872.2:n.3145+7500G>A
|
|
|
NM_138694.4:c.10253C>T
MANE Select
|
NP_619639.3:p.Ala3418Val
|
|