|
ENST00000375254.8:c.15273T>C
MANE Select
|
ENSP00000364403.3:p.Arg5091=
|
|
|
ENST00000375224.1:c.2394T>C
|
ENSP00000364372.1:p.Arg798=
|
|
|
ENST00000375225.7:c.498T>C
|
ENSP00000364373.3:p.Arg166=
|
|
|
ENST00000375254.7:c.15273T>C
|
ENSP00000364403.3:p.Arg5091=
|
|
|
ENST00000459947.5:n.3280T>C
|
|
|
|
NM_020765.2:c.15273T>C
|
NP_065816.2:p.Arg5091=
|
|
|
XM_011541108.1:c.15426T>C
|
XP_011539410.1:p.Arg5142=
|
|
|
XM_011541109.1:c.15423T>C
|
XP_011539411.1:p.Arg5141=
|
|
|
XM_011541110.1:c.15423T>C
|
XP_011539412.1:p.Arg5141=
|
|
|
XM_011541111.1:c.15423T>C
|
XP_011539413.1:p.Arg5141=
|
|
|
XM_011541112.1:c.15411T>C
|
XP_011539414.1:p.Arg5137=
|
|
|
XM_011541113.1:c.15408T>C
|
XP_011539415.1:p.Arg5136=
|
|
|
XM_011541114.1:c.15408T>C
|
XP_011539416.1:p.Arg5136=
|
|
|
XM_011541115.1:c.15402T>C
|
XP_011539417.1:p.Arg5134=
|
|
|
XM_011541116.1:c.15393T>C
|
XP_011539418.1:p.Arg5131=
|
|
|
XM_011541117.1:c.15342T>C
|
XP_011539419.1:p.Arg5114=
|
|
|
XM_011541118.1:c.15339T>C
|
XP_011539420.1:p.Arg5113=
|
|
|
XM_011541119.1:c.15306T>C
|
XP_011539421.1:p.Arg5102=
|
|
|
XM_011541120.1:c.15303T>C
|
XP_011539422.1:p.Arg5101=
|
|
|
XM_011541121.1:c.15270T>C
|
XP_011539423.1:p.Arg5090=
|
|
|
XM_011541108.3:c.15540T>C
|
XP_011539410.2:p.Arg5180=
|
|
|
XM_011541109.3:c.15537T>C
|
XP_011539411.2:p.Arg5179=
|
|
|
XM_011541110.3:c.15537T>C
|
XP_011539412.2:p.Arg5179=
|
|
|
XM_011541111.3:c.15537T>C
|
XP_011539413.2:p.Arg5179=
|
|
|
XM_011541112.3:c.15525T>C
|
XP_011539414.2:p.Arg5175=
|
|
|
XM_011541113.3:c.15522T>C
|
XP_011539415.2:p.Arg5174=
|
|
|
XM_011541114.3:c.15522T>C
|
XP_011539416.2:p.Arg5174=
|
|
|
XM_011541115.3:c.15516T>C
|
XP_011539417.2:p.Arg5172=
|
|
|
XM_011541116.3:c.15507T>C
|
XP_011539418.2:p.Arg5169=
|
|
|
XM_011541117.3:c.15456T>C
|
XP_011539419.2:p.Arg5152=
|
|
|
XM_011541118.3:c.15453T>C
|
XP_011539420.2:p.Arg5151=
|
|
|
XM_011541119.3:c.15420T>C
|
XP_011539421.2:p.Arg5140=
|
|
|
XM_011541120.3:c.15417T>C
|
XP_011539422.2:p.Arg5139=
|
|
|
XM_011541121.3:c.15384T>C
|
XP_011539423.2:p.Arg5128=
|
|
|
XM_017000822.2:c.15519T>C
|
XP_016856311.2:p.Arg5173=
|
|
|
XM_017000823.2:c.15492T>C
|
XP_016856312.2:p.Arg5164=
|
|
|
XM_017000824.2:c.15438T>C
|
XP_016856313.2:p.Arg5146=
|
|
|
XM_017000825.2:c.15423T>C
|
XP_016856314.2:p.Arg5141=
|
|
|
XM_017000826.2:c.15420T>C
|
XP_016856315.2:p.Arg5140=
|
|
|
XM_017000827.2:c.15405T>C
|
XP_016856316.2:p.Arg5135=
|
|
|
XM_017000828.2:c.15381T>C
|
XP_016856317.2:p.Arg5127=
|
|
|
XM_017000829.2:c.15333T>C
|
XP_016856318.2:p.Arg5111=
|
|
|
XM_017000830.2:c.15282T>C
|
XP_016856319.2:p.Arg5094=
|
|
|
NM_020765.3:c.15273T>C
MANE Select
|
NP_065816.2:p.Arg5091=
|
|
