ENST00000397676.8:c.342C>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ala114=
|
|
ENST00000397676.7:c.342C>G
(ALG3)
|
ENSP00000380793.3:p.Ala114=
|
|
ENST00000411922.5:c.242C>G
(ALG3)
|
ENSP00000394917.1:p.Pro81Arg
|
|
ENST00000414845.5:c.235C>G
(ALG3)
|
|
|
ENST00000423996.5:c.*107C>G
(ALG3)
|
ENSP00000407011.1:n.*107C>G
|
|
ENST00000444495.1:c.2106+100863G>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100863G>C
|
|
ENST00000445626.6:c.198C>G
(ALG3)
|
ENSP00000402744.2:p.Ala66=
|
|
ENST00000446569.1:c.155-212C>G
(ALG3)
|
|
|
ENST00000455059.5:c.222C>G
(ALG3)
|
ENSP00000397613.1:p.Ala74=
|
|
ENST00000461415.5:n.315C>G
(ALG3)
|
|
|
ENST00000482048.1:n.331C>G
(ALG3)
|
|
|
ENST00000488976.5:n.227C>G
(ALG3)
|
|
|
NM_001006941.2:c.198C>G
(ALG3)
|
NP_001006942.1:p.Ala66=
|
|
NM_005787.5:c.342C>G
(ALG3)
|
NP_005778.1:p.Ala114=
|
|
NR_024533.1:n.273C>G
(ALG3)
|
|
|
NR_024534.1:n.336C>G
(ALG3)
|
|
|
XM_011512322.1:c.243C>G
(ALG3)
|
XP_011510624.1:p.Ala81=
|
|
XM_011512323.1:c.222C>G
(ALG3)
|
XP_011510625.1:p.Ala74=
|
|
XM_011512323.2:c.222C>G
(ALG3)
|
XP_011510625.1:p.Ala74=
|
|
XM_024453296.1:c.120C>G
(ALG3)
|
XP_024309064.1:p.Ala40=
|
|
NM_005787.6:c.342C>G
(ALG3)
MANE Select
|
NP_005778.1:p.Ala114=
|
|