ENST00000371117.8:c.10913G>T
MANE Select
|
ENSP00000360158.3:p.Arg3638Met
|
|
ENST00000371117.7:c.10913G>T
|
ENSP00000360158.3:p.Arg3638Met
|
|
NM_138694.3:c.10913G>T
|
NP_619639.3:p.Arg3638Met
|
|
XM_011514679.1:c.10913G>T
|
XP_011512981.1:p.Arg3638Met
|
|
XM_011514680.1:c.10913G>T
|
XP_011512982.1:p.Arg3638Met
|
|
XM_011514681.1:c.10784G>T
|
XP_011512983.1:p.Arg3595Met
|
|
XM_011514682.1:c.10775G>T
|
XP_011512984.1:p.Arg3592Met
|
|
XM_011514683.1:c.10271G>T
|
XP_011512985.1:p.Arg3424Met
|
|
XM_011514684.1:c.10202G>T
|
XP_011512986.1:p.Arg3401Met
|
|
XM_011514687.1:c.10157-9993G>T
|
XP_011512989.1:n.10157-9993G>T
|
|
XM_011514690.1:c.4988G>T
|
XP_011512992.1:p.Arg1663Met
|
|
XM_011514691.1:c.4988G>T
|
XP_011512993.1:p.Arg1663Met
|
|
XR_926870.1:n.535+6840C>A
|
|
|
XR_926871.1:n.403+6840C>A
|
|
|
XR_926872.1:n.535+6840C>A
|
|
|
XM_011514680.3:c.10913G>T
|
XP_011512982.1:p.Arg3638Met
|
|
XM_011514682.3:c.10775G>T
|
XP_011512984.1:p.Arg3592Met
|
|
XM_011514683.3:c.10271G>T
|
XP_011512985.1:p.Arg3424Met
|
|
XM_011514684.3:c.10202G>T
|
XP_011512986.1:p.Arg3401Met
|
|
XM_011514690.3:c.4988G>T
|
XP_011512992.1:p.Arg1663Met
|
|
XM_011514691.3:c.4988G>T
|
XP_011512993.1:p.Arg1663Met
|
|
XM_017010944.2:c.10913G>T
|
XP_016866433.1:p.Arg3638Met
|
|
XM_017010945.2:c.10838G>T
|
XP_016866434.1:p.Arg3613Met
|
|
XM_017010946.2:c.10718G>T
|
XP_016866435.1:p.Arg3573Met
|
|
XM_017010947.2:c.10649G>T
|
XP_016866436.1:p.Arg3550Met
|
|
XM_017010948.2:c.10202G>T
|
XP_016866437.1:p.Arg3401Met
|
|
XM_017010949.2:c.9053G>T
|
XP_016866438.1:p.Arg3018Met
|
|
XR_001743469.1:n.11189G>T
|
|
|
XR_001744157.1:n.3145+6840C>A
|
|
|
XR_926870.2:n.3145+6840C>A
|
|
|
XR_926871.2:n.3013+6840C>A
|
|
|
XR_926872.2:n.3145+6840C>A
|
|
|
NM_138694.4:c.10913G>T
MANE Select
|
NP_619639.3:p.Arg3638Met
|
|