ENST00000270357.10:c.1519T>G
MANE Select
|
ENSP00000270357.4:p.Phe507Val
|
|
ENST00000270357.8:c.826T>G
|
ENSP00000270357.3:p.Phe276Val
|
|
ENST00000437406.1:c.110-25T>G
|
ENSP00000403319.1:n.110-25T>G
|
|
ENST00000451363.5:c.160T>G
|
ENSP00000414661.1:p.Phe54Val
|
|
ENST00000464550.5:n.355T>G
|
|
|
ENST00000471657.1:n.322T>G
|
|
|
ENST00000481757.5:n.2453T>G
|
|
|
ENST00000486058.5:n.1632T>G
|
|
|
ENST00000493398.5:n.665T>G
|
|
|
NM_018226.4:c.1519T>G
|
NP_060696.4:p.Phe507Val
|
|
XM_005247036.3:c.1511-25T>G
|
XP_005247093.1:n.1511-25T>G
|
|
NM_018226.5:c.1519T>G
|
NP_060696.4:p.Phe507Val
|
|
XM_005247036.4:c.1511-25T>G
|
XP_005247093.1:n.1511-25T>G
|
|
NM_018226.6:c.1519T>G
MANE Select
|
NP_060696.4:p.Phe507Val
|
|