ENST00000371117.8:c.11782G>T
MANE Select
|
ENSP00000360158.3:p.Glu3928Ter
|
|
ENST00000371117.7:c.11782G>T
|
ENSP00000360158.3:p.Glu3928Ter
|
|
NM_138694.3:c.11782G>T
|
NP_619639.3:p.Glu3928Ter
|
|
XM_011514679.1:c.11782G>T
|
XP_011512981.1:p.Glu3928Ter
|
|
XM_011514680.1:c.11782G>T
|
XP_011512982.1:p.Glu3928Ter
|
|
XM_011514681.1:c.11653G>T
|
XP_011512983.1:p.Glu3885Ter
|
|
XM_011514682.1:c.11644G>T
|
XP_011512984.1:p.Glu3882Ter
|
|
XM_011514683.1:c.11140G>T
|
XP_011512985.1:p.Glu3714Ter
|
|
XM_011514684.1:c.11071G>T
|
XP_011512986.1:p.Glu3691Ter
|
|
XM_011514690.1:c.5857G>T
|
XP_011512992.1:p.Glu1953Ter
|
|
XM_011514691.1:c.5857G>T
|
XP_011512993.1:p.Glu1953Ter
|
|
XM_011514680.3:c.11782G>T
|
XP_011512982.1:p.Glu3928Ter
|
|
XM_011514682.3:c.11644G>T
|
XP_011512984.1:p.Glu3882Ter
|
|
XM_011514683.3:c.11140G>T
|
XP_011512985.1:p.Glu3714Ter
|
|
XM_011514684.3:c.11071G>T
|
XP_011512986.1:p.Glu3691Ter
|
|
XM_011514690.3:c.5857G>T
|
XP_011512992.1:p.Glu1953Ter
|
|
XM_011514691.3:c.5857G>T
|
XP_011512993.1:p.Glu1953Ter
|
|
XM_017010944.2:c.11782G>T
|
XP_016866433.1:p.Glu3928Ter
|
|
XM_017010945.2:c.11707G>T
|
XP_016866434.1:p.Glu3903Ter
|
|
XM_017010946.2:c.11587G>T
|
XP_016866435.1:p.Glu3863Ter
|
|
XM_017010947.2:c.11518G>T
|
XP_016866436.1:p.Glu3840Ter
|
|
XM_017010948.2:c.11071G>T
|
XP_016866437.1:p.Glu3691Ter
|
|
XM_017010949.2:c.9922G>T
|
XP_016866438.1:p.Glu3308Ter
|
|
NM_138694.4:c.11782G>T
MANE Select
|
NP_619639.3:p.Glu3928Ter
|
|