ENST00000397676.8:c.590G>T
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Gly197Val
|
|
ENST00000397676.7:c.590G>T
(ALG3)
|
ENSP00000380793.3:p.Gly197Val
|
|
ENST00000411922.5:c.*166G>T
(ALG3)
|
ENSP00000394917.1:n.*166G>T
|
|
ENST00000414845.5:c.337+255G>T
(ALG3)
|
|
|
ENST00000423996.5:c.*355G>T
(ALG3)
|
ENSP00000407011.1:n.*355G>T
|
|
ENST00000444495.1:c.2106+100506C>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100506C>A
|
|
ENST00000445626.6:c.446G>T
(ALG3)
|
ENSP00000402744.2:p.Gly149Val
|
|
ENST00000446569.1:c.300G>T
(ALG3)
|
|
|
ENST00000455059.5:c.470G>T
(ALG3)
|
ENSP00000397613.1:p.Gly157Val
|
|
ENST00000461415.5:n.563G>T
(ALG3)
|
|
|
ENST00000477959.1:n.130G>T
(ALG3)
|
|
|
ENST00000482048.1:n.579G>T
(ALG3)
|
|
|
ENST00000488976.5:n.475G>T
(ALG3)
|
|
|
NM_001006941.2:c.446G>T
(ALG3)
|
NP_001006942.1:p.Gly149Val
|
|
NM_005787.5:c.590G>T
(ALG3)
|
NP_005778.1:p.Gly197Val
|
|
NR_024533.1:n.521G>T
(ALG3)
|
|
|
NR_024534.1:n.584G>T
(ALG3)
|
|
|
XM_011512322.1:c.491G>T
(ALG3)
|
XP_011510624.1:p.Gly164Val
|
|
XM_011512323.1:c.470G>T
(ALG3)
|
XP_011510625.1:p.Gly157Val
|
|
XM_011512323.2:c.470G>T
(ALG3)
|
XP_011510625.1:p.Gly157Val
|
|
XM_024453296.1:c.368G>T
(ALG3)
|
XP_024309064.1:p.Gly123Val
|
|
NM_005787.6:c.590G>T
(ALG3)
MANE Select
|
NP_005778.1:p.Gly197Val
|
|