ENST00000397676.8:c.601T>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Phe201Val
|
|
ENST00000397676.7:c.601T>G
(ALG3)
|
ENSP00000380793.3:p.Phe201Val
|
|
ENST00000411922.5:c.*177T>G
(ALG3)
|
ENSP00000394917.1:n.*177T>G
|
|
ENST00000414845.5:c.337+266T>G
(ALG3)
|
|
|
ENST00000423996.5:c.*366T>G
(ALG3)
|
ENSP00000407011.1:n.*366T>G
|
|
ENST00000444495.1:c.2106+100495A>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100495A>C
|
|
ENST00000445626.6:c.457T>G
(ALG3)
|
ENSP00000402744.2:p.Phe153Val
|
|
ENST00000446569.1:c.311T>G
(ALG3)
|
|
|
ENST00000455059.5:c.481T>G
(ALG3)
|
ENSP00000397613.1:p.Phe161Val
|
|
ENST00000461415.5:n.574T>G
(ALG3)
|
|
|
ENST00000477959.1:n.141T>G
(ALG3)
|
|
|
ENST00000482048.1:n.590T>G
(ALG3)
|
|
|
ENST00000488976.5:n.486T>G
(ALG3)
|
|
|
NM_001006941.2:c.457T>G
(ALG3)
|
NP_001006942.1:p.Phe153Val
|
|
NM_005787.5:c.601T>G
(ALG3)
|
NP_005778.1:p.Phe201Val
|
|
NR_024533.1:n.532T>G
(ALG3)
|
|
|
NR_024534.1:n.595T>G
(ALG3)
|
|
|
XM_011512322.1:c.502T>G
(ALG3)
|
XP_011510624.1:p.Phe168Val
|
|
XM_011512323.1:c.481T>G
(ALG3)
|
XP_011510625.1:p.Phe161Val
|
|
XM_011512323.2:c.481T>G
(ALG3)
|
XP_011510625.1:p.Phe161Val
|
|
XM_024453296.1:c.379T>G
(ALG3)
|
XP_024309064.1:p.Phe127Val
|
|
NM_005787.6:c.601T>G
(ALG3)
MANE Select
|
NP_005778.1:p.Phe201Val
|
|