ENST00000270357.10:c.1606C>G
MANE Select
|
ENSP00000270357.4:p.Leu536Val
|
|
ENST00000270357.8:c.913C>G
|
ENSP00000270357.3:p.Leu305Val
|
|
ENST00000437406.1:c.172C>G
|
ENSP00000403319.1:p.Leu58Val
|
|
ENST00000451363.5:c.247C>G
|
ENSP00000414661.1:p.Leu83Val
|
|
ENST00000464550.5:n.442C>G
|
|
|
ENST00000471657.1:n.409C>G
|
|
|
ENST00000481757.5:n.2540C>G
|
|
|
ENST00000486058.5:n.1719C>G
|
|
|
ENST00000493398.5:n.752C>G
|
|
|
NM_018226.4:c.1606C>G
|
NP_060696.4:p.Leu536Val
|
|
XM_005247036.3:c.1573C>G
|
XP_005247093.1:p.Leu525Val
|
|
NM_018226.5:c.1606C>G
|
NP_060696.4:p.Leu536Val
|
|
XM_005247036.4:c.1573C>G
|
XP_005247093.1:p.Leu525Val
|
|
NM_018226.6:c.1606C>G
MANE Select
|
NP_060696.4:p.Leu536Val
|
|