ENST00000397676.8:c.556A>T
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ile186Phe
|
|
ENST00000397676.7:c.556A>T
(ALG3)
|
ENSP00000380793.3:p.Ile186Phe
|
|
ENST00000411922.5:c.*132A>T
(ALG3)
|
ENSP00000394917.1:n.*132A>T
|
|
ENST00000414845.5:c.337+221A>T
(ALG3)
|
|
|
ENST00000423996.5:c.*321A>T
(ALG3)
|
ENSP00000407011.1:n.*321A>T
|
|
ENST00000444495.1:c.2106+100540T>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100540T>A
|
|
ENST00000445626.6:c.412A>T
(ALG3)
|
ENSP00000402744.2:p.Ile138Phe
|
|
ENST00000446569.1:c.266A>T
(ALG3)
|
|
|
ENST00000455059.5:c.436A>T
(ALG3)
|
ENSP00000397613.1:p.Ile146Phe
|
|
ENST00000461415.5:n.529A>T
(ALG3)
|
|
|
ENST00000477959.1:n.96A>T
(ALG3)
|
|
|
ENST00000482048.1:n.545A>T
(ALG3)
|
|
|
ENST00000488976.5:n.441A>T
(ALG3)
|
|
|
NM_001006941.2:c.412A>T
(ALG3)
|
NP_001006942.1:p.Ile138Phe
|
|
NM_005787.5:c.556A>T
(ALG3)
|
NP_005778.1:p.Ile186Phe
|
|
NR_024533.1:n.487A>T
(ALG3)
|
|
|
NR_024534.1:n.550A>T
(ALG3)
|
|
|
XM_011512322.1:c.457A>T
(ALG3)
|
XP_011510624.1:p.Ile153Phe
|
|
XM_011512323.1:c.436A>T
(ALG3)
|
XP_011510625.1:p.Ile146Phe
|
|
XM_011512323.2:c.436A>T
(ALG3)
|
XP_011510625.1:p.Ile146Phe
|
|
XM_024453296.1:c.334A>T
(ALG3)
|
XP_024309064.1:p.Ile112Phe
|
|
NM_005787.6:c.556A>T
(ALG3)
MANE Select
|
NP_005778.1:p.Ile186Phe
|
|