ENST00000397676.8:c.602T>A
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Phe201Tyr
|
|
ENST00000397676.7:c.602T>A
(ALG3)
|
ENSP00000380793.3:p.Phe201Tyr
|
|
ENST00000411922.5:c.*178T>A
(ALG3)
|
ENSP00000394917.1:n.*178T>A
|
|
ENST00000414845.5:c.337+267T>A
(ALG3)
|
|
|
ENST00000423996.5:c.*367T>A
(ALG3)
|
ENSP00000407011.1:n.*367T>A
|
|
ENST00000444495.1:c.2106+100494A>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+100494A>T
|
|
ENST00000445626.6:c.458T>A
(ALG3)
|
ENSP00000402744.2:p.Phe153Tyr
|
|
ENST00000446569.1:c.312T>A
(ALG3)
|
|
|
ENST00000455059.5:c.482T>A
(ALG3)
|
ENSP00000397613.1:p.Phe161Tyr
|
|
ENST00000461415.5:n.575T>A
(ALG3)
|
|
|
ENST00000477959.1:n.142T>A
(ALG3)
|
|
|
ENST00000482048.1:n.591T>A
(ALG3)
|
|
|
ENST00000488976.5:n.487T>A
(ALG3)
|
|
|
NM_001006941.2:c.458T>A
(ALG3)
|
NP_001006942.1:p.Phe153Tyr
|
|
NM_005787.5:c.602T>A
(ALG3)
|
NP_005778.1:p.Phe201Tyr
|
|
NR_024533.1:n.533T>A
(ALG3)
|
|
|
NR_024534.1:n.596T>A
(ALG3)
|
|
|
XM_011512322.1:c.503T>A
(ALG3)
|
XP_011510624.1:p.Phe168Tyr
|
|
XM_011512323.1:c.482T>A
(ALG3)
|
XP_011510625.1:p.Phe161Tyr
|
|
XM_011512323.2:c.482T>A
(ALG3)
|
XP_011510625.1:p.Phe161Tyr
|
|
XM_024453296.1:c.380T>A
(ALG3)
|
XP_024309064.1:p.Phe127Tyr
|
|
NM_005787.6:c.602T>A
(ALG3)
MANE Select
|
NP_005778.1:p.Phe201Tyr
|
|