ENST00000397676.8:c.598T>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Phe200Val
|
|
ENST00000397676.7:c.598T>G
(ALG3)
|
ENSP00000380793.3:p.Phe200Val
|
|
ENST00000411922.5:c.*174T>G
(ALG3)
|
ENSP00000394917.1:n.*174T>G
|
|
ENST00000414845.5:c.337+263T>G
(ALG3)
|
|
|
ENST00000423996.5:c.*363T>G
(ALG3)
|
ENSP00000407011.1:n.*363T>G
|
|
ENST00000444495.1:c.2106+100498A>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100498A>C
|
|
ENST00000445626.6:c.454T>G
(ALG3)
|
ENSP00000402744.2:p.Phe152Val
|
|
ENST00000446569.1:c.308T>G
(ALG3)
|
|
|
ENST00000455059.5:c.478T>G
(ALG3)
|
ENSP00000397613.1:p.Phe160Val
|
|
ENST00000461415.5:n.571T>G
(ALG3)
|
|
|
ENST00000477959.1:n.138T>G
(ALG3)
|
|
|
ENST00000482048.1:n.587T>G
(ALG3)
|
|
|
ENST00000488976.5:n.483T>G
(ALG3)
|
|
|
NM_001006941.2:c.454T>G
(ALG3)
|
NP_001006942.1:p.Phe152Val
|
|
NM_005787.5:c.598T>G
(ALG3)
|
NP_005778.1:p.Phe200Val
|
|
NR_024533.1:n.529T>G
(ALG3)
|
|
|
NR_024534.1:n.592T>G
(ALG3)
|
|
|
XM_011512322.1:c.499T>G
(ALG3)
|
XP_011510624.1:p.Phe167Val
|
|
XM_011512323.1:c.478T>G
(ALG3)
|
XP_011510625.1:p.Phe160Val
|
|
XM_011512323.2:c.478T>G
(ALG3)
|
XP_011510625.1:p.Phe160Val
|
|
XM_024453296.1:c.376T>G
(ALG3)
|
XP_024309064.1:p.Phe126Val
|
|
NM_005787.6:c.598T>G
(ALG3)
MANE Select
|
NP_005778.1:p.Phe200Val
|
|