ENST00000397676.8:c.589G>C
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Gly197Arg
|
|
ENST00000397676.7:c.589G>C
(ALG3)
|
ENSP00000380793.3:p.Gly197Arg
|
|
ENST00000411922.5:c.*165G>C
(ALG3)
|
ENSP00000394917.1:n.*165G>C
|
|
ENST00000414845.5:c.337+254G>C
(ALG3)
|
|
|
ENST00000423996.5:c.*354G>C
(ALG3)
|
ENSP00000407011.1:n.*354G>C
|
|
ENST00000444495.1:c.2106+100507C>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+100507C>G
|
|
ENST00000445626.6:c.445G>C
(ALG3)
|
ENSP00000402744.2:p.Gly149Arg
|
|
ENST00000446569.1:c.299G>C
(ALG3)
|
|
|
ENST00000455059.5:c.469G>C
(ALG3)
|
ENSP00000397613.1:p.Gly157Arg
|
|
ENST00000461415.5:n.562G>C
(ALG3)
|
|
|
ENST00000477959.1:n.129G>C
(ALG3)
|
|
|
ENST00000482048.1:n.578G>C
(ALG3)
|
|
|
ENST00000488976.5:n.474G>C
(ALG3)
|
|
|
NM_001006941.2:c.445G>C
(ALG3)
|
NP_001006942.1:p.Gly149Arg
|
|
NM_005787.5:c.589G>C
(ALG3)
|
NP_005778.1:p.Gly197Arg
|
|
NR_024533.1:n.520G>C
(ALG3)
|
|
|
NR_024534.1:n.583G>C
(ALG3)
|
|
|
XM_011512322.1:c.490G>C
(ALG3)
|
XP_011510624.1:p.Gly164Arg
|
|
XM_011512323.1:c.469G>C
(ALG3)
|
XP_011510625.1:p.Gly157Arg
|
|
XM_011512323.2:c.469G>C
(ALG3)
|
XP_011510625.1:p.Gly157Arg
|
|
XM_024453296.1:c.367G>C
(ALG3)
|
XP_024309064.1:p.Gly123Arg
|
|
NM_005787.6:c.589G>C
(ALG3)
MANE Select
|
NP_005778.1:p.Gly197Arg
|
|