ENST00000397676.8:c.389T>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Val130Gly
|
|
ENST00000397676.7:c.389T>G
(ALG3)
|
ENSP00000380793.3:p.Val130Gly
|
|
ENST00000411922.5:c.289T>G
(ALG3)
|
ENSP00000394917.1:p.Cys97Gly
|
|
ENST00000414845.5:c.282T>G
(ALG3)
|
|
|
ENST00000423996.5:c.*154T>G
(ALG3)
|
ENSP00000407011.1:n.*154T>G
|
|
ENST00000444495.1:c.2106+100816A>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100816A>C
|
|
ENST00000445626.6:c.245T>G
(ALG3)
|
ENSP00000402744.2:p.Val82Gly
|
|
ENST00000446569.1:c.155-165T>G
(ALG3)
|
|
|
ENST00000455059.5:c.269T>G
(ALG3)
|
ENSP00000397613.1:p.Val90Gly
|
|
ENST00000461415.5:n.362T>G
(ALG3)
|
|
|
ENST00000482048.1:n.378T>G
(ALG3)
|
|
|
ENST00000488976.5:n.274T>G
(ALG3)
|
|
|
NM_001006941.2:c.245T>G
(ALG3)
|
NP_001006942.1:p.Val82Gly
|
|
NM_005787.5:c.389T>G
(ALG3)
|
NP_005778.1:p.Val130Gly
|
|
NR_024533.1:n.320T>G
(ALG3)
|
|
|
NR_024534.1:n.383T>G
(ALG3)
|
|
|
XM_011512322.1:c.290T>G
(ALG3)
|
XP_011510624.1:p.Val97Gly
|
|
XM_011512323.1:c.269T>G
(ALG3)
|
XP_011510625.1:p.Val90Gly
|
|
XM_011512323.2:c.269T>G
(ALG3)
|
XP_011510625.1:p.Val90Gly
|
|
XM_024453296.1:c.167T>G
(ALG3)
|
XP_024309064.1:p.Val56Gly
|
|
NM_005787.6:c.389T>G
(ALG3)
MANE Select
|
NP_005778.1:p.Val130Gly
|
|