ENST00000397676.8:c.605G>T
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ser202Ile
|
|
ENST00000397676.7:c.605G>T
(ALG3)
|
ENSP00000380793.3:p.Ser202Ile
|
|
ENST00000411922.5:c.*181G>T
(ALG3)
|
ENSP00000394917.1:n.*181G>T
|
|
ENST00000414845.5:c.337+270G>T
(ALG3)
|
|
|
ENST00000423996.5:c.*370G>T
(ALG3)
|
ENSP00000407011.1:n.*370G>T
|
|
ENST00000444495.1:c.2106+100491C>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100491C>A
|
|
ENST00000445626.6:c.461G>T
(ALG3)
|
ENSP00000402744.2:p.Ser154Ile
|
|
ENST00000446569.1:c.315G>T
(ALG3)
|
|
|
ENST00000455059.5:c.485G>T
(ALG3)
|
ENSP00000397613.1:p.Ser162Ile
|
|
ENST00000461415.5:n.578G>T
(ALG3)
|
|
|
ENST00000477959.1:n.145G>T
(ALG3)
|
|
|
ENST00000482048.1:n.594G>T
(ALG3)
|
|
|
ENST00000488976.5:n.490G>T
(ALG3)
|
|
|
NM_001006941.2:c.461G>T
(ALG3)
|
NP_001006942.1:p.Ser154Ile
|
|
NM_005787.5:c.605G>T
(ALG3)
|
NP_005778.1:p.Ser202Ile
|
|
NR_024533.1:n.536G>T
(ALG3)
|
|
|
NR_024534.1:n.599G>T
(ALG3)
|
|
|
XM_011512322.1:c.506G>T
(ALG3)
|
XP_011510624.1:p.Ser169Ile
|
|
XM_011512323.1:c.485G>T
(ALG3)
|
XP_011510625.1:p.Ser162Ile
|
|
XM_011512323.2:c.485G>T
(ALG3)
|
XP_011510625.1:p.Ser162Ile
|
|
XM_024453296.1:c.383G>T
(ALG3)
|
XP_024309064.1:p.Ser128Ile
|
|
NM_005787.6:c.605G>T
(ALG3)
MANE Select
|
NP_005778.1:p.Ser202Ile
|
|