ENST00000371117.8:c.10942A>T
MANE Select
|
ENSP00000360158.3:p.Arg3648Trp
|
|
ENST00000371117.7:c.10942A>T
|
ENSP00000360158.3:p.Arg3648Trp
|
|
NM_138694.3:c.10942A>T
|
NP_619639.3:p.Arg3648Trp
|
|
XM_011514679.1:c.10942A>T
|
XP_011512981.1:p.Arg3648Trp
|
|
XM_011514680.1:c.10942A>T
|
XP_011512982.1:p.Arg3648Trp
|
|
XM_011514681.1:c.10813A>T
|
XP_011512983.1:p.Arg3605Trp
|
|
XM_011514682.1:c.10804A>T
|
XP_011512984.1:p.Arg3602Trp
|
|
XM_011514683.1:c.10300A>T
|
XP_011512985.1:p.Arg3434Trp
|
|
XM_011514684.1:c.10231A>T
|
XP_011512986.1:p.Arg3411Trp
|
|
XM_011514687.1:c.10157-9964A>T
|
XP_011512989.1:n.10157-9964A>T
|
|
XM_011514690.1:c.5017A>T
|
XP_011512992.1:p.Arg1673Trp
|
|
XM_011514691.1:c.5017A>T
|
XP_011512993.1:p.Arg1673Trp
|
|
XR_926870.1:n.535+6811T>A
|
|
|
XR_926871.1:n.403+6811T>A
|
|
|
XR_926872.1:n.535+6811T>A
|
|
|
XM_011514680.3:c.10942A>T
|
XP_011512982.1:p.Arg3648Trp
|
|
XM_011514682.3:c.10804A>T
|
XP_011512984.1:p.Arg3602Trp
|
|
XM_011514683.3:c.10300A>T
|
XP_011512985.1:p.Arg3434Trp
|
|
XM_011514684.3:c.10231A>T
|
XP_011512986.1:p.Arg3411Trp
|
|
XM_011514690.3:c.5017A>T
|
XP_011512992.1:p.Arg1673Trp
|
|
XM_011514691.3:c.5017A>T
|
XP_011512993.1:p.Arg1673Trp
|
|
XM_017010944.2:c.10942A>T
|
XP_016866433.1:p.Arg3648Trp
|
|
XM_017010945.2:c.10867A>T
|
XP_016866434.1:p.Arg3623Trp
|
|
XM_017010946.2:c.10747A>T
|
XP_016866435.1:p.Arg3583Trp
|
|
XM_017010947.2:c.10678A>T
|
XP_016866436.1:p.Arg3560Trp
|
|
XM_017010948.2:c.10231A>T
|
XP_016866437.1:p.Arg3411Trp
|
|
XM_017010949.2:c.9082A>T
|
XP_016866438.1:p.Arg3028Trp
|
|
XR_001743469.1:n.11218A>T
|
|
|
XR_001744157.1:n.3145+6811T>A
|
|
|
XR_926870.2:n.3145+6811T>A
|
|
|
XR_926871.2:n.3013+6811T>A
|
|
|
XR_926872.2:n.3145+6811T>A
|
|
|
NM_138694.4:c.10942A>T
MANE Select
|
NP_619639.3:p.Arg3648Trp
|
|