ENST00000270357.10:c.1618T>C
MANE Select
|
ENSP00000270357.4:p.Trp540Arg
|
|
ENST00000270357.8:c.925T>C
|
ENSP00000270357.3:p.Trp309Arg
|
|
ENST00000437406.1:c.184T>C
|
ENSP00000403319.1:p.Trp62Arg
|
|
ENST00000451363.5:c.259T>C
|
ENSP00000414661.1:p.Trp87Arg
|
|
ENST00000464550.5:n.454T>C
|
|
|
ENST00000471657.1:n.421T>C
|
|
|
ENST00000481757.5:n.2552T>C
|
|
|
ENST00000486058.5:n.1731T>C
|
|
|
ENST00000493398.5:n.764T>C
|
|
|
NM_018226.4:c.1618T>C
|
NP_060696.4:p.Trp540Arg
|
|
XM_005247036.3:c.1585T>C
|
XP_005247093.1:p.Trp529Arg
|
|
NM_018226.5:c.1618T>C
|
NP_060696.4:p.Trp540Arg
|
|
XM_005247036.4:c.1585T>C
|
XP_005247093.1:p.Trp529Arg
|
|
NM_018226.6:c.1618T>C
MANE Select
|
NP_060696.4:p.Trp540Arg
|
|