ENST00000397676.8:c.602T>C
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Phe201Ser
|
|
ENST00000397676.7:c.602T>C
(ALG3)
|
ENSP00000380793.3:p.Phe201Ser
|
|
ENST00000411922.5:c.*178T>C
(ALG3)
|
ENSP00000394917.1:n.*178T>C
|
|
ENST00000414845.5:c.337+267T>C
(ALG3)
|
|
|
ENST00000423996.5:c.*367T>C
(ALG3)
|
ENSP00000407011.1:n.*367T>C
|
|
ENST00000444495.1:c.2106+100494A>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+100494A>G
|
|
ENST00000445626.6:c.458T>C
(ALG3)
|
ENSP00000402744.2:p.Phe153Ser
|
|
ENST00000446569.1:c.312T>C
(ALG3)
|
|
|
ENST00000455059.5:c.482T>C
(ALG3)
|
ENSP00000397613.1:p.Phe161Ser
|
|
ENST00000461415.5:n.575T>C
(ALG3)
|
|
|
ENST00000477959.1:n.142T>C
(ALG3)
|
|
|
ENST00000482048.1:n.591T>C
(ALG3)
|
|
|
ENST00000488976.5:n.487T>C
(ALG3)
|
|
|
NM_001006941.2:c.458T>C
(ALG3)
|
NP_001006942.1:p.Phe153Ser
|
|
NM_005787.5:c.602T>C
(ALG3)
|
NP_005778.1:p.Phe201Ser
|
|
NR_024533.1:n.533T>C
(ALG3)
|
|
|
NR_024534.1:n.596T>C
(ALG3)
|
|
|
XM_011512322.1:c.503T>C
(ALG3)
|
XP_011510624.1:p.Phe168Ser
|
|
XM_011512323.1:c.482T>C
(ALG3)
|
XP_011510625.1:p.Phe161Ser
|
|
XM_011512323.2:c.482T>C
(ALG3)
|
XP_011510625.1:p.Phe161Ser
|
|
XM_024453296.1:c.380T>C
(ALG3)
|
XP_024309064.1:p.Phe127Ser
|
|
NM_005787.6:c.602T>C
(ALG3)
MANE Select
|
NP_005778.1:p.Phe201Ser
|
|