ENST00000350721.9:c.6267A>C
MANE Select
|
ENSP00000343741.4:p.Arg2089=
|
|
ENST00000513291.2:n.1451A>C
|
|
|
ENST00000654170.1:n.1110A>C
|
|
|
ENST00000656590.1:c.5057A>C
|
|
|
ENST00000661310.1:c.6075A>C
|
ENSP00000499589.1:p.Arg2025=
|
|
ENST00000665483.1:n.122A>C
|
|
|
ENST00000666447.1:n.102A>C
|
|
|
ENST00000666943.1:n.1731A>C
|
|
|
ENST00000350721.8:c.6267A>C
|
ENSP00000343741.4:p.Arg2089=
|
|
NM_001184.3:c.6267A>C
|
NP_001175.2:p.Arg2089=
|
|
XM_011512924.1:c.6273A>C
|
XP_011511226.1:p.Arg2091=
|
|
XM_011512925.1:c.6081A>C
|
XP_011511227.1:p.Arg2027=
|
|
XR_924147.1:n.6362A>C
|
|
|
XR_924148.1:n.6362A>C
|
|
|
XR_924149.1:n.6241A>C
|
|
|
NM_001354579.1:c.6075A>C
|
NP_001341508.1:p.Arg2025=
|
|
XR_001740179.2:n.6356A>C
|
|
|
XR_001740180.2:n.6410A>C
|
|
|
XR_001740181.2:n.6289A>C
|
|
|
XR_001740182.1:n.6241A>C
|
|
|
XR_002959543.1:n.6466A>C
|
|
|
XR_924148.2:n.6362A>C
|
|
|
NM_001184.4:c.6267A>C
MANE Select
|
NP_001175.2:p.Arg2089=
|
|
NM_001354579.2:c.6075A>C
|
NP_001341508.1:p.Arg2025=
|
|