ENST00000397676.8:c.596G>A
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Cys199Tyr
|
|
ENST00000397676.7:c.596G>A
(ALG3)
|
ENSP00000380793.3:p.Cys199Tyr
|
|
ENST00000411922.5:c.*172G>A
(ALG3)
|
ENSP00000394917.1:n.*172G>A
|
|
ENST00000414845.5:c.337+261G>A
(ALG3)
|
|
|
ENST00000423996.5:c.*361G>A
(ALG3)
|
ENSP00000407011.1:n.*361G>A
|
|
ENST00000444495.1:c.2106+100500C>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+100500C>T
|
|
ENST00000445626.6:c.452G>A
(ALG3)
|
ENSP00000402744.2:p.Cys151Tyr
|
|
ENST00000446569.1:c.306G>A
(ALG3)
|
|
|
ENST00000455059.5:c.476G>A
(ALG3)
|
ENSP00000397613.1:p.Cys159Tyr
|
|
ENST00000461415.5:n.569G>A
(ALG3)
|
|
|
ENST00000477959.1:n.136G>A
(ALG3)
|
|
|
ENST00000482048.1:n.585G>A
(ALG3)
|
|
|
ENST00000488976.5:n.481G>A
(ALG3)
|
|
|
NM_001006941.2:c.452G>A
(ALG3)
|
NP_001006942.1:p.Cys151Tyr
|
|
NM_005787.5:c.596G>A
(ALG3)
|
NP_005778.1:p.Cys199Tyr
|
|
NR_024533.1:n.527G>A
(ALG3)
|
|
|
NR_024534.1:n.590G>A
(ALG3)
|
|
|
XM_011512322.1:c.497G>A
(ALG3)
|
XP_011510624.1:p.Cys166Tyr
|
|
XM_011512323.1:c.476G>A
(ALG3)
|
XP_011510625.1:p.Cys159Tyr
|
|
XM_011512323.2:c.476G>A
(ALG3)
|
XP_011510625.1:p.Cys159Tyr
|
|
XM_024453296.1:c.374G>A
(ALG3)
|
XP_024309064.1:p.Cys125Tyr
|
|
NM_005787.6:c.596G>A
(ALG3)
MANE Select
|
NP_005778.1:p.Cys199Tyr
|
|