ENST00000397676.8:c.496T>C
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ser166Pro
|
|
ENST00000397676.7:c.496T>C
(ALG3)
|
ENSP00000380793.3:p.Ser166Pro
|
|
ENST00000411922.5:c.*72T>C
(ALG3)
|
ENSP00000394917.1:n.*72T>C
|
|
ENST00000414845.5:c.337+161T>C
(ALG3)
|
|
|
ENST00000423996.5:c.*261T>C
(ALG3)
|
ENSP00000407011.1:n.*261T>C
|
|
ENST00000444495.1:c.2106+100600A>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+100600A>G
|
|
ENST00000445626.6:c.352T>C
(ALG3)
|
ENSP00000402744.2:p.Ser118Pro
|
|
ENST00000446569.1:c.206T>C
(ALG3)
|
|
|
ENST00000455059.5:c.376T>C
(ALG3)
|
ENSP00000397613.1:p.Ser126Pro
|
|
ENST00000461415.5:n.469T>C
(ALG3)
|
|
|
ENST00000477959.1:n.36T>C
(ALG3)
|
|
|
ENST00000482048.1:n.485T>C
(ALG3)
|
|
|
ENST00000488976.5:n.381T>C
(ALG3)
|
|
|
NM_001006941.2:c.352T>C
(ALG3)
|
NP_001006942.1:p.Ser118Pro
|
|
NM_005787.5:c.496T>C
(ALG3)
|
NP_005778.1:p.Ser166Pro
|
|
NR_024533.1:n.427T>C
(ALG3)
|
|
|
NR_024534.1:n.490T>C
(ALG3)
|
|
|
XM_011512322.1:c.397T>C
(ALG3)
|
XP_011510624.1:p.Ser133Pro
|
|
XM_011512323.1:c.376T>C
(ALG3)
|
XP_011510625.1:p.Ser126Pro
|
|
XM_011512323.2:c.376T>C
(ALG3)
|
XP_011510625.1:p.Ser126Pro
|
|
XM_024453296.1:c.274T>C
(ALG3)
|
XP_024309064.1:p.Ser92Pro
|
|
NM_005787.6:c.496T>C
(ALG3)
MANE Select
|
NP_005778.1:p.Ser166Pro
|
|