ENST00000397676.8:c.604A>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ser202Gly
|
|
ENST00000397676.7:c.604A>G
(ALG3)
|
ENSP00000380793.3:p.Ser202Gly
|
|
ENST00000411922.5:c.*180A>G
(ALG3)
|
ENSP00000394917.1:n.*180A>G
|
|
ENST00000414845.5:c.337+269A>G
(ALG3)
|
|
|
ENST00000423996.5:c.*369A>G
(ALG3)
|
ENSP00000407011.1:n.*369A>G
|
|
ENST00000444495.1:c.2106+100492T>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100492T>C
|
|
ENST00000445626.6:c.460A>G
(ALG3)
|
ENSP00000402744.2:p.Ser154Gly
|
|
ENST00000446569.1:c.314A>G
(ALG3)
|
|
|
ENST00000455059.5:c.484A>G
(ALG3)
|
ENSP00000397613.1:p.Ser162Gly
|
|
ENST00000461415.5:n.577A>G
(ALG3)
|
|
|
ENST00000477959.1:n.144A>G
(ALG3)
|
|
|
ENST00000482048.1:n.593A>G
(ALG3)
|
|
|
ENST00000488976.5:n.489A>G
(ALG3)
|
|
|
NM_001006941.2:c.460A>G
(ALG3)
|
NP_001006942.1:p.Ser154Gly
|
|
NM_005787.5:c.604A>G
(ALG3)
|
NP_005778.1:p.Ser202Gly
|
|
NR_024533.1:n.535A>G
(ALG3)
|
|
|
NR_024534.1:n.598A>G
(ALG3)
|
|
|
XM_011512322.1:c.505A>G
(ALG3)
|
XP_011510624.1:p.Ser169Gly
|
|
XM_011512323.1:c.484A>G
(ALG3)
|
XP_011510625.1:p.Ser162Gly
|
|
XM_011512323.2:c.484A>G
(ALG3)
|
XP_011510625.1:p.Ser162Gly
|
|
XM_024453296.1:c.382A>G
(ALG3)
|
XP_024309064.1:p.Ser128Gly
|
|
NM_005787.6:c.604A>G
(ALG3)
MANE Select
|
NP_005778.1:p.Ser202Gly
|
|