ENST00000682338.1:c.1288T>G
|
ENSP00000507062.1:p.Phe430Val
|
|
ENST00000682793.1:c.1288T>G
|
ENSP00000506910.1:p.Phe430Val
|
|
ENST00000682838.1:c.*1030T>G
|
ENSP00000507652.1:n.*1030T>G
|
|
ENST00000683578.1:c.1288T>G
|
ENSP00000507430.1:p.Phe430Val
|
|
ENST00000683606.1:n.903T>G
|
|
|
ENST00000683661.1:n.2823T>G
|
|
|
ENST00000684324.1:c.1288T>G
|
ENSP00000507937.1:p.Phe430Val
|
|
ENST00000684545.1:c.1288T>G
|
ENSP00000506733.1:p.Phe430Val
|
|
ENST00000684624.1:n.665T>G
|
|
|
ENST00000684714.1:c.1288T>G
|
ENSP00000506861.1:p.Phe430Val
|
|
ENST00000684731.1:n.749T>G
|
|
|
ENST00000375679.9:c.1288T>G
MANE Select
|
ENSP00000364831.5:p.Phe430Val
|
|
ENST00000375667.7:c.781T>G
|
ENSP00000364819.3:p.Phe261Val
|
|
ENST00000375679.8:c.1288T>G
|
ENSP00000364831.4:p.Phe430Val
|
|
ENST00000619181.4:c.907T>G
|
ENSP00000483866.1:p.Phe303Val
|
|
NM_000085.4:c.1288T>G
|
NP_000076.2:p.Phe430Val
|
|
NM_001165945.2:c.781T>G
|
NP_001159417.2:p.Phe261Val
|
|
XM_011540619.1:c.1129T>G
|
XP_011538921.1:p.Phe377Val
|
|
XM_011540620.1:c.1288T>G
|
XP_011538922.1:p.Phe430Val
|
|
XM_011540621.1:c.637T>G
|
XP_011538923.1:p.Phe213Val
|
|
NM_000085.5:c.1288T>G
MANE Select
|
NP_000076.2:p.Phe430Val
|
|