ENST00000397676.8:c.521A=
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Asn174=
|
|
ENST00000397676.7:c.521A=
(ALG3)
|
ENSP00000380793.3:p.Asn174=
|
|
ENST00000411922.5:c.*97A=
(ALG3)
|
ENSP00000394917.1:n.*97A=
|
|
ENST00000414845.5:c.337+186A=
(ALG3)
|
|
|
ENST00000423996.5:c.*286A=
(ALG3)
|
ENSP00000407011.1:n.*286A=
|
|
ENST00000444495.1:c.2106+100575T=
(EIF2B5)
|
ENSP00000409142.1:n.2106+100575T=
|
|
ENST00000445626.6:c.377A=
(ALG3)
|
ENSP00000402744.2:p.Asn126=
|
|
ENST00000446569.1:c.231A=
(ALG3)
|
|
|
ENST00000455059.5:c.401A=
(ALG3)
|
ENSP00000397613.1:p.Asn134=
|
|
ENST00000461415.5:n.494A=
(ALG3)
|
|
|
ENST00000477959.1:n.61A=
(ALG3)
|
|
|
ENST00000482048.1:n.510A=
(ALG3)
|
|
|
ENST00000488976.5:n.406A=
(ALG3)
|
|
|
NM_001006941.2:c.377A=
(ALG3)
|
NP_001006942.1:p.Asn126=
|
|
NM_005787.5:c.521A=
(ALG3)
|
NP_005778.1:p.Asn174=
|
|
NR_024533.1:n.452A=
(ALG3)
|
|
|
NR_024534.1:n.515A=
(ALG3)
|
|
|
XM_011512322.1:c.422A=
(ALG3)
|
XP_011510624.1:p.Asn141=
|
|
XM_011512323.1:c.401A=
(ALG3)
|
XP_011510625.1:p.Asn134=
|
|
XM_011512323.2:c.401A=
(ALG3)
|
XP_011510625.1:p.Asn134=
|
|
XM_024453296.1:c.299A=
(ALG3)
|
XP_024309064.1:p.Asn100=
|
|
NM_005787.6:c.521A=
(ALG3)
MANE Select
|
NP_005778.1:p.Asn174=
|
|