ENST00000270357.10:c.1617G>C
MANE Select
|
ENSP00000270357.4:p.Leu539=
|
|
ENST00000270357.8:c.924G>C
|
ENSP00000270357.3:p.Leu308=
|
|
ENST00000437406.1:c.183G>C
|
ENSP00000403319.1:p.Leu61=
|
|
ENST00000451363.5:c.258G>C
|
ENSP00000414661.1:p.Leu86=
|
|
ENST00000464550.5:n.453G>C
|
|
|
ENST00000471657.1:n.420G>C
|
|
|
ENST00000481757.5:n.2551G>C
|
|
|
ENST00000486058.5:n.1730G>C
|
|
|
ENST00000493398.5:n.763G>C
|
|
|
NM_018226.4:c.1617G>C
|
NP_060696.4:p.Leu539=
|
|
XM_005247036.3:c.1584G>C
|
XP_005247093.1:p.Leu528=
|
|
NM_018226.5:c.1617G>C
|
NP_060696.4:p.Leu539=
|
|
XM_005247036.4:c.1584G>C
|
XP_005247093.1:p.Leu528=
|
|
NM_018226.6:c.1617G>C
MANE Select
|
NP_060696.4:p.Leu539=
|
|