ENST00000397676.8:c.534C>A
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ala178=
|
|
ENST00000397676.7:c.534C>A
(ALG3)
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ENSP00000380793.3:p.Ala178=
|
|
ENST00000411922.5:c.*110C>A
(ALG3)
|
ENSP00000394917.1:n.*110C>A
|
|
ENST00000414845.5:c.337+199C>A
(ALG3)
|
|
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ENST00000423996.5:c.*299C>A
(ALG3)
|
ENSP00000407011.1:n.*299C>A
|
|
ENST00000444495.1:c.2106+100562G>T
(EIF2B5)
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ENSP00000409142.1:n.2106+100562G>T
|
|
ENST00000445626.6:c.390C>A
(ALG3)
|
ENSP00000402744.2:p.Ala130=
|
|
ENST00000446569.1:c.244C>A
(ALG3)
|
|
|
ENST00000455059.5:c.414C>A
(ALG3)
|
ENSP00000397613.1:p.Ala138=
|
|
ENST00000461415.5:n.507C>A
(ALG3)
|
|
|
ENST00000477959.1:n.74C>A
(ALG3)
|
|
|
ENST00000482048.1:n.523C>A
(ALG3)
|
|
|
ENST00000488976.5:n.419C>A
(ALG3)
|
|
|
NM_001006941.2:c.390C>A
(ALG3)
|
NP_001006942.1:p.Ala130=
|
|
NM_005787.5:c.534C>A
(ALG3)
|
NP_005778.1:p.Ala178=
|
|
NR_024533.1:n.465C>A
(ALG3)
|
|
|
NR_024534.1:n.528C>A
(ALG3)
|
|
|
XM_011512322.1:c.435C>A
(ALG3)
|
XP_011510624.1:p.Ala145=
|
|
XM_011512323.1:c.414C>A
(ALG3)
|
XP_011510625.1:p.Ala138=
|
|
XM_011512323.2:c.414C>A
(ALG3)
|
XP_011510625.1:p.Ala138=
|
|
XM_024453296.1:c.312C>A
(ALG3)
|
XP_024309064.1:p.Ala104=
|
|
NM_005787.6:c.534C>A
(ALG3)
MANE Select
|
NP_005778.1:p.Ala178=
|
|