ENST00000270357.10:c.1615C>G
MANE Select
|
ENSP00000270357.4:p.Leu539Val
|
|
ENST00000270357.8:c.922C>G
|
ENSP00000270357.3:p.Leu308Val
|
|
ENST00000437406.1:c.181C>G
|
ENSP00000403319.1:p.Leu61Val
|
|
ENST00000451363.5:c.256C>G
|
ENSP00000414661.1:p.Leu86Val
|
|
ENST00000464550.5:n.451C>G
|
|
|
ENST00000471657.1:n.418C>G
|
|
|
ENST00000481757.5:n.2549C>G
|
|
|
ENST00000486058.5:n.1728C>G
|
|
|
ENST00000493398.5:n.761C>G
|
|
|
NM_018226.4:c.1615C>G
|
NP_060696.4:p.Leu539Val
|
|
XM_005247036.3:c.1582C>G
|
XP_005247093.1:p.Leu528Val
|
|
NM_018226.5:c.1615C>G
|
NP_060696.4:p.Leu539Val
|
|
XM_005247036.4:c.1582C>G
|
XP_005247093.1:p.Leu528Val
|
|
NM_018226.6:c.1615C>G
MANE Select
|
NP_060696.4:p.Leu539Val
|
|