ENST00000397676.8:c.599T>C
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Phe200Ser
|
|
ENST00000397676.7:c.599T>C
(ALG3)
|
ENSP00000380793.3:p.Phe200Ser
|
|
ENST00000411922.5:c.*175T>C
(ALG3)
|
ENSP00000394917.1:n.*175T>C
|
|
ENST00000414845.5:c.337+264T>C
(ALG3)
|
|
|
ENST00000423996.5:c.*364T>C
(ALG3)
|
ENSP00000407011.1:n.*364T>C
|
|
ENST00000444495.1:c.2106+100497A>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+100497A>G
|
|
ENST00000445626.6:c.455T>C
(ALG3)
|
ENSP00000402744.2:p.Phe152Ser
|
|
ENST00000446569.1:c.309T>C
(ALG3)
|
|
|
ENST00000455059.5:c.479T>C
(ALG3)
|
ENSP00000397613.1:p.Phe160Ser
|
|
ENST00000461415.5:n.572T>C
(ALG3)
|
|
|
ENST00000477959.1:n.139T>C
(ALG3)
|
|
|
ENST00000482048.1:n.588T>C
(ALG3)
|
|
|
ENST00000488976.5:n.484T>C
(ALG3)
|
|
|
NM_001006941.2:c.455T>C
(ALG3)
|
NP_001006942.1:p.Phe152Ser
|
|
NM_005787.5:c.599T>C
(ALG3)
|
NP_005778.1:p.Phe200Ser
|
|
NR_024533.1:n.530T>C
(ALG3)
|
|
|
NR_024534.1:n.593T>C
(ALG3)
|
|
|
XM_011512322.1:c.500T>C
(ALG3)
|
XP_011510624.1:p.Phe167Ser
|
|
XM_011512323.1:c.479T>C
(ALG3)
|
XP_011510625.1:p.Phe160Ser
|
|
XM_011512323.2:c.479T>C
(ALG3)
|
XP_011510625.1:p.Phe160Ser
|
|
XM_024453296.1:c.377T>C
(ALG3)
|
XP_024309064.1:p.Phe126Ser
|
|
NM_005787.6:c.599T>C
(ALG3)
MANE Select
|
NP_005778.1:p.Phe200Ser
|
|