ENST00000371117.8:c.11691A>G
MANE Select
|
ENSP00000360158.3:p.Glu3897=
|
|
ENST00000371117.7:c.11691A>G
|
ENSP00000360158.3:p.Glu3897=
|
|
NM_138694.3:c.11691A>G
|
NP_619639.3:p.Glu3897=
|
|
XM_011514679.1:c.11691A>G
|
XP_011512981.1:p.Glu3897=
|
|
XM_011514680.1:c.11691A>G
|
XP_011512982.1:p.Glu3897=
|
|
XM_011514681.1:c.11562A>G
|
XP_011512983.1:p.Glu3854=
|
|
XM_011514682.1:c.11553A>G
|
XP_011512984.1:p.Glu3851=
|
|
XM_011514683.1:c.11049A>G
|
XP_011512985.1:p.Glu3683=
|
|
XM_011514684.1:c.10980A>G
|
XP_011512986.1:p.Glu3660=
|
|
XM_011514690.1:c.5766A>G
|
XP_011512992.1:p.Glu1922=
|
|
XM_011514691.1:c.5766A>G
|
XP_011512993.1:p.Glu1922=
|
|
XM_011514680.3:c.11691A>G
|
XP_011512982.1:p.Glu3897=
|
|
XM_011514682.3:c.11553A>G
|
XP_011512984.1:p.Glu3851=
|
|
XM_011514683.3:c.11049A>G
|
XP_011512985.1:p.Glu3683=
|
|
XM_011514684.3:c.10980A>G
|
XP_011512986.1:p.Glu3660=
|
|
XM_011514690.3:c.5766A>G
|
XP_011512992.1:p.Glu1922=
|
|
XM_011514691.3:c.5766A>G
|
XP_011512993.1:p.Glu1922=
|
|
XM_017010944.2:c.11691A>G
|
XP_016866433.1:p.Glu3897=
|
|
XM_017010945.2:c.11616A>G
|
XP_016866434.1:p.Glu3872=
|
|
XM_017010946.2:c.11496A>G
|
XP_016866435.1:p.Glu3832=
|
|
XM_017010947.2:c.11427A>G
|
XP_016866436.1:p.Glu3809=
|
|
XM_017010948.2:c.10980A>G
|
XP_016866437.1:p.Glu3660=
|
|
XM_017010949.2:c.9831A>G
|
XP_016866438.1:p.Glu3277=
|
|
NM_138694.4:c.11691A>G
MANE Select
|
NP_619639.3:p.Glu3897=
|
|