ENST00000371117.8:c.11060A>G
MANE Select
|
ENSP00000360158.3:p.Gln3687Arg
|
|
ENST00000371117.7:c.11060A>G
|
ENSP00000360158.3:p.Gln3687Arg
|
|
NM_138694.3:c.11060A>G
|
NP_619639.3:p.Gln3687Arg
|
|
XM_011514679.1:c.11060A>G
|
XP_011512981.1:p.Gln3687Arg
|
|
XM_011514680.1:c.11060A>G
|
XP_011512982.1:p.Gln3687Arg
|
|
XM_011514681.1:c.10931A>G
|
XP_011512983.1:p.Gln3644Arg
|
|
XM_011514682.1:c.10922A>G
|
XP_011512984.1:p.Gln3641Arg
|
|
XM_011514683.1:c.10418A>G
|
XP_011512985.1:p.Gln3473Arg
|
|
XM_011514684.1:c.10349A>G
|
XP_011512986.1:p.Gln3450Arg
|
|
XM_011514687.1:c.10157-9846A>G
|
XP_011512989.1:n.10157-9846A>G
|
|
XM_011514690.1:c.5135A>G
|
XP_011512992.1:p.Gln1712Arg
|
|
XM_011514691.1:c.5135A>G
|
XP_011512993.1:p.Gln1712Arg
|
|
XR_926870.1:n.535+6693T>C
|
|
|
XR_926871.1:n.403+6693T>C
|
|
|
XR_926872.1:n.535+6693T>C
|
|
|
XM_011514680.3:c.11060A>G
|
XP_011512982.1:p.Gln3687Arg
|
|
XM_011514682.3:c.10922A>G
|
XP_011512984.1:p.Gln3641Arg
|
|
XM_011514683.3:c.10418A>G
|
XP_011512985.1:p.Gln3473Arg
|
|
XM_011514684.3:c.10349A>G
|
XP_011512986.1:p.Gln3450Arg
|
|
XM_011514690.3:c.5135A>G
|
XP_011512992.1:p.Gln1712Arg
|
|
XM_011514691.3:c.5135A>G
|
XP_011512993.1:p.Gln1712Arg
|
|
XM_017010944.2:c.11060A>G
|
XP_016866433.1:p.Gln3687Arg
|
|
XM_017010945.2:c.10985A>G
|
XP_016866434.1:p.Gln3662Arg
|
|
XM_017010946.2:c.10865A>G
|
XP_016866435.1:p.Gln3622Arg
|
|
XM_017010947.2:c.10796A>G
|
XP_016866436.1:p.Gln3599Arg
|
|
XM_017010948.2:c.10349A>G
|
XP_016866437.1:p.Gln3450Arg
|
|
XM_017010949.2:c.9200A>G
|
XP_016866438.1:p.Gln3067Arg
|
|
XR_001743469.1:n.11336A>G
|
|
|
XR_001744157.1:n.3145+6693T>C
|
|
|
XR_926870.2:n.3145+6693T>C
|
|
|
XR_926871.2:n.3013+6693T>C
|
|
|
XR_926872.2:n.3145+6693T>C
|
|
|
NM_138694.4:c.11060A>G
MANE Select
|
NP_619639.3:p.Gln3687Arg
|
|