ENST00000371117.8:c.10928A>T
MANE Select
|
ENSP00000360158.3:p.Glu3643Val
|
|
ENST00000371117.7:c.10928A>T
|
ENSP00000360158.3:p.Glu3643Val
|
|
NM_138694.3:c.10928A>T
|
NP_619639.3:p.Glu3643Val
|
|
XM_011514679.1:c.10928A>T
|
XP_011512981.1:p.Glu3643Val
|
|
XM_011514680.1:c.10928A>T
|
XP_011512982.1:p.Glu3643Val
|
|
XM_011514681.1:c.10799A>T
|
XP_011512983.1:p.Glu3600Val
|
|
XM_011514682.1:c.10790A>T
|
XP_011512984.1:p.Glu3597Val
|
|
XM_011514683.1:c.10286A>T
|
XP_011512985.1:p.Glu3429Val
|
|
XM_011514684.1:c.10217A>T
|
XP_011512986.1:p.Glu3406Val
|
|
XM_011514687.1:c.10157-9978A>T
|
XP_011512989.1:n.10157-9978A>T
|
|
XM_011514690.1:c.5003A>T
|
XP_011512992.1:p.Glu1668Val
|
|
XM_011514691.1:c.5003A>T
|
XP_011512993.1:p.Glu1668Val
|
|
XR_926870.1:n.535+6825T>A
|
|
|
XR_926871.1:n.403+6825T>A
|
|
|
XR_926872.1:n.535+6825T>A
|
|
|
XM_011514680.3:c.10928A>T
|
XP_011512982.1:p.Glu3643Val
|
|
XM_011514682.3:c.10790A>T
|
XP_011512984.1:p.Glu3597Val
|
|
XM_011514683.3:c.10286A>T
|
XP_011512985.1:p.Glu3429Val
|
|
XM_011514684.3:c.10217A>T
|
XP_011512986.1:p.Glu3406Val
|
|
XM_011514690.3:c.5003A>T
|
XP_011512992.1:p.Glu1668Val
|
|
XM_011514691.3:c.5003A>T
|
XP_011512993.1:p.Glu1668Val
|
|
XM_017010944.2:c.10928A>T
|
XP_016866433.1:p.Glu3643Val
|
|
XM_017010945.2:c.10853A>T
|
XP_016866434.1:p.Glu3618Val
|
|
XM_017010946.2:c.10733A>T
|
XP_016866435.1:p.Glu3578Val
|
|
XM_017010947.2:c.10664A>T
|
XP_016866436.1:p.Glu3555Val
|
|
XM_017010948.2:c.10217A>T
|
XP_016866437.1:p.Glu3406Val
|
|
XM_017010949.2:c.9068A>T
|
XP_016866438.1:p.Glu3023Val
|
|
XR_001743469.1:n.11204A>T
|
|
|
XR_001744157.1:n.3145+6825T>A
|
|
|
XR_926870.2:n.3145+6825T>A
|
|
|
XR_926871.2:n.3013+6825T>A
|
|
|
XR_926872.2:n.3145+6825T>A
|
|
|
NM_138694.4:c.10928A>T
MANE Select
|
NP_619639.3:p.Glu3643Val
|
|