ENST00000397676.8:c.577C>T
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Arg193Cys
|
|
ENST00000397676.7:c.577C>T
(ALG3)
|
ENSP00000380793.3:p.Arg193Cys
|
|
ENST00000411922.5:c.*153C>T
(ALG3)
|
ENSP00000394917.1:n.*153C>T
|
|
ENST00000414845.5:c.337+242C>T
(ALG3)
|
|
|
ENST00000423996.5:c.*342C>T
(ALG3)
|
ENSP00000407011.1:n.*342C>T
|
|
ENST00000444495.1:c.2106+100519G>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100519G>A
|
|
ENST00000445626.6:c.433C>T
(ALG3)
|
ENSP00000402744.2:p.Arg145Cys
|
|
ENST00000446569.1:c.287C>T
(ALG3)
|
|
|
ENST00000455059.5:c.457C>T
(ALG3)
|
ENSP00000397613.1:p.Arg153Cys
|
|
ENST00000461415.5:n.550C>T
(ALG3)
|
|
|
ENST00000477959.1:n.117C>T
(ALG3)
|
|
|
ENST00000482048.1:n.566C>T
(ALG3)
|
|
|
ENST00000488976.5:n.462C>T
(ALG3)
|
|
|
NM_001006941.2:c.433C>T
(ALG3)
|
NP_001006942.1:p.Arg145Cys
|
|
NM_005787.5:c.577C>T
(ALG3)
|
NP_005778.1:p.Arg193Cys
|
|
NR_024533.1:n.508C>T
(ALG3)
|
|
|
NR_024534.1:n.571C>T
(ALG3)
|
|
|
XM_011512322.1:c.478C>T
(ALG3)
|
XP_011510624.1:p.Arg160Cys
|
|
XM_011512323.1:c.457C>T
(ALG3)
|
XP_011510625.1:p.Arg153Cys
|
|
XM_011512323.2:c.457C>T
(ALG3)
|
XP_011510625.1:p.Arg153Cys
|
|
XM_024453296.1:c.355C>T
(ALG3)
|
XP_024309064.1:p.Arg119Cys
|
|
NM_005787.6:c.577C>T
(ALG3)
MANE Select
|
NP_005778.1:p.Arg193Cys
|
|