ENST00000270357.10:c.1633C>G
MANE Select
|
ENSP00000270357.4:p.Leu545Val
|
|
ENST00000270357.8:c.940C>G
|
ENSP00000270357.3:p.Leu314Val
|
|
ENST00000437406.1:c.199C>G
|
ENSP00000403319.1:p.Leu67Val
|
|
ENST00000451363.5:c.274C>G
|
ENSP00000414661.1:p.Leu92Val
|
|
ENST00000464550.5:n.469C>G
|
|
|
ENST00000471657.1:n.436C>G
|
|
|
ENST00000481757.5:n.2567C>G
|
|
|
ENST00000486058.5:n.1746C>G
|
|
|
ENST00000493398.5:n.779C>G
|
|
|
NM_018226.4:c.1633C>G
|
NP_060696.4:p.Leu545Val
|
|
XM_005247036.3:c.1600C>G
|
XP_005247093.1:p.Leu534Val
|
|
NM_018226.5:c.1633C>G
|
NP_060696.4:p.Leu545Val
|
|
XM_005247036.4:c.1600C>G
|
XP_005247093.1:p.Leu534Val
|
|
NM_018226.6:c.1633C>G
MANE Select
|
NP_060696.4:p.Leu545Val
|
|