ENST00000397676.8:c.341C>A
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Ala114Asp
|
|
ENST00000397676.7:c.341C>A
(ALG3)
|
ENSP00000380793.3:p.Ala114Asp
|
|
ENST00000411922.5:c.241C>A
(ALG3)
|
ENSP00000394917.1:p.Pro81Thr
|
|
ENST00000414845.5:c.234C>A
(ALG3)
|
|
|
ENST00000423996.5:c.*106C>A
(ALG3)
|
ENSP00000407011.1:n.*106C>A
|
|
ENST00000444495.1:c.2106+100864G>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+100864G>T
|
|
ENST00000445626.6:c.197C>A
(ALG3)
|
ENSP00000402744.2:p.Ala66Asp
|
|
ENST00000446569.1:c.155-213C>A
(ALG3)
|
|
|
ENST00000455059.5:c.221C>A
(ALG3)
|
ENSP00000397613.1:p.Ala74Asp
|
|
ENST00000461415.5:n.314C>A
(ALG3)
|
|
|
ENST00000482048.1:n.330C>A
(ALG3)
|
|
|
ENST00000488976.5:n.226C>A
(ALG3)
|
|
|
NM_001006941.2:c.197C>A
(ALG3)
|
NP_001006942.1:p.Ala66Asp
|
|
NM_005787.5:c.341C>A
(ALG3)
|
NP_005778.1:p.Ala114Asp
|
|
NR_024533.1:n.272C>A
(ALG3)
|
|
|
NR_024534.1:n.335C>A
(ALG3)
|
|
|
XM_011512322.1:c.242C>A
(ALG3)
|
XP_011510624.1:p.Ala81Asp
|
|
XM_011512323.1:c.221C>A
(ALG3)
|
XP_011510625.1:p.Ala74Asp
|
|
XM_011512323.2:c.221C>A
(ALG3)
|
XP_011510625.1:p.Ala74Asp
|
|
XM_024453296.1:c.119C>A
(ALG3)
|
XP_024309064.1:p.Ala40Asp
|
|
NM_005787.6:c.341C>A
(ALG3)
MANE Select
|
NP_005778.1:p.Ala114Asp
|
|