ENST00000270357.10:c.1609T>G
MANE Select
|
ENSP00000270357.4:p.Phe537Val
|
|
ENST00000270357.8:c.916T>G
|
ENSP00000270357.3:p.Phe306Val
|
|
ENST00000437406.1:c.175T>G
|
ENSP00000403319.1:p.Phe59Val
|
|
ENST00000451363.5:c.250T>G
|
ENSP00000414661.1:p.Phe84Val
|
|
ENST00000464550.5:n.445T>G
|
|
|
ENST00000471657.1:n.412T>G
|
|
|
ENST00000481757.5:n.2543T>G
|
|
|
ENST00000486058.5:n.1722T>G
|
|
|
ENST00000493398.5:n.755T>G
|
|
|
NM_018226.4:c.1609T>G
|
NP_060696.4:p.Phe537Val
|
|
XM_005247036.3:c.1576T>G
|
XP_005247093.1:p.Phe526Val
|
|
NM_018226.5:c.1609T>G
|
NP_060696.4:p.Phe537Val
|
|
XM_005247036.4:c.1576T>G
|
XP_005247093.1:p.Phe526Val
|
|
NM_018226.6:c.1609T>G
MANE Select
|
NP_060696.4:p.Phe537Val
|
|