ENST00000270357.10:c.1552C>G
MANE Select
|
ENSP00000270357.4:p.Leu518Val
|
|
ENST00000270357.8:c.859C>G
|
ENSP00000270357.3:p.Leu287Val
|
|
ENST00000437406.1:c.118C>G
|
ENSP00000403319.1:p.Leu40Val
|
|
ENST00000451363.5:c.193C>G
|
ENSP00000414661.1:p.Leu65Val
|
|
ENST00000464550.5:n.388C>G
|
|
|
ENST00000471657.1:n.355C>G
|
|
|
ENST00000481757.5:n.2486C>G
|
|
|
ENST00000486058.5:n.1665C>G
|
|
|
ENST00000493398.5:n.698C>G
|
|
|
NM_018226.4:c.1552C>G
|
NP_060696.4:p.Leu518Val
|
|
XM_005247036.3:c.1519C>G
|
XP_005247093.1:p.Leu507Val
|
|
NM_018226.5:c.1552C>G
|
NP_060696.4:p.Leu518Val
|
|
XM_005247036.4:c.1519C>G
|
XP_005247093.1:p.Leu507Val
|
|
NM_018226.6:c.1552C>G
MANE Select
|
NP_060696.4:p.Leu518Val
|
|