ENST00000397676.8:c.423G>A
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Leu141=
|
|
ENST00000397676.7:c.423G>A
(ALG3)
|
ENSP00000380793.3:p.Leu141=
|
|
ENST00000411922.5:c.323G>A
(ALG3)
|
ENSP00000394917.1:p.Ter108=
|
|
ENST00000414845.5:c.316G>A
(ALG3)
|
|
|
ENST00000423996.5:c.*188G>A
(ALG3)
|
ENSP00000407011.1:n.*188G>A
|
|
ENST00000444495.1:c.2106+100782C>T
(EIF2B5)
|
ENSP00000409142.1:n.2106+100782C>T
|
|
ENST00000445626.6:c.279G>A
(ALG3)
|
ENSP00000402744.2:p.Leu93=
|
|
ENST00000446569.1:c.155-131G>A
(ALG3)
|
|
|
ENST00000455059.5:c.303G>A
(ALG3)
|
ENSP00000397613.1:p.Leu101=
|
|
ENST00000461415.5:n.396G>A
(ALG3)
|
|
|
ENST00000482048.1:n.412G>A
(ALG3)
|
|
|
ENST00000488976.5:n.308G>A
(ALG3)
|
|
|
NM_001006941.2:c.279G>A
(ALG3)
|
NP_001006942.1:p.Leu93=
|
|
NM_005787.5:c.423G>A
(ALG3)
|
NP_005778.1:p.Leu141=
|
|
NR_024533.1:n.354G>A
(ALG3)
|
|
|
NR_024534.1:n.417G>A
(ALG3)
|
|
|
XM_011512322.1:c.324G>A
(ALG3)
|
XP_011510624.1:p.Leu108=
|
|
XM_011512323.1:c.303G>A
(ALG3)
|
XP_011510625.1:p.Leu101=
|
|
XM_011512323.2:c.303G>A
(ALG3)
|
XP_011510625.1:p.Leu101=
|
|
XM_024453296.1:c.201G>A
(ALG3)
|
XP_024309064.1:p.Leu67=
|
|
NM_005787.6:c.423G>A
(ALG3)
MANE Select
|
NP_005778.1:p.Leu141=
|
|