ENST00000397676.8:c.503T>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Phe168Cys
|
|
ENST00000397676.7:c.503T>G
(ALG3)
|
ENSP00000380793.3:p.Phe168Cys
|
|
ENST00000411922.5:c.*79T>G
(ALG3)
|
ENSP00000394917.1:n.*79T>G
|
|
ENST00000414845.5:c.337+168T>G
(ALG3)
|
|
|
ENST00000423996.5:c.*268T>G
(ALG3)
|
ENSP00000407011.1:n.*268T>G
|
|
ENST00000444495.1:c.2106+100593A>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100593A>C
|
|
ENST00000445626.6:c.359T>G
(ALG3)
|
ENSP00000402744.2:p.Phe120Cys
|
|
ENST00000446569.1:c.213T>G
(ALG3)
|
|
|
ENST00000455059.5:c.383T>G
(ALG3)
|
ENSP00000397613.1:p.Phe128Cys
|
|
ENST00000461415.5:n.476T>G
(ALG3)
|
|
|
ENST00000477959.1:n.43T>G
(ALG3)
|
|
|
ENST00000482048.1:n.492T>G
(ALG3)
|
|
|
ENST00000488976.5:n.388T>G
(ALG3)
|
|
|
NM_001006941.2:c.359T>G
(ALG3)
|
NP_001006942.1:p.Phe120Cys
|
|
NM_005787.5:c.503T>G
(ALG3)
|
NP_005778.1:p.Phe168Cys
|
|
NR_024533.1:n.434T>G
(ALG3)
|
|
|
NR_024534.1:n.497T>G
(ALG3)
|
|
|
XM_011512322.1:c.404T>G
(ALG3)
|
XP_011510624.1:p.Phe135Cys
|
|
XM_011512323.1:c.383T>G
(ALG3)
|
XP_011510625.1:p.Phe128Cys
|
|
XM_011512323.2:c.383T>G
(ALG3)
|
XP_011510625.1:p.Phe128Cys
|
|
XM_024453296.1:c.281T>G
(ALG3)
|
XP_024309064.1:p.Phe94Cys
|
|
NM_005787.6:c.503T>G
(ALG3)
MANE Select
|
NP_005778.1:p.Phe168Cys
|
|