ENST00000397676.8:c.394T>C
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Tyr132His
|
|
ENST00000397676.7:c.394T>C
(ALG3)
|
ENSP00000380793.3:p.Tyr132His
|
|
ENST00000411922.5:c.294T>C
(ALG3)
|
ENSP00000394917.1:p.Ser98=
|
|
ENST00000414845.5:c.287T>C
(ALG3)
|
|
|
ENST00000423996.5:c.*159T>C
(ALG3)
|
ENSP00000407011.1:n.*159T>C
|
|
ENST00000444495.1:c.2106+100811A>G
(EIF2B5)
|
ENSP00000409142.1:n.2106+100811A>G
|
|
ENST00000445626.6:c.250T>C
(ALG3)
|
ENSP00000402744.2:p.Tyr84His
|
|
ENST00000446569.1:c.155-160T>C
(ALG3)
|
|
|
ENST00000455059.5:c.274T>C
(ALG3)
|
ENSP00000397613.1:p.Tyr92His
|
|
ENST00000461415.5:n.367T>C
(ALG3)
|
|
|
ENST00000482048.1:n.383T>C
(ALG3)
|
|
|
ENST00000488976.5:n.279T>C
(ALG3)
|
|
|
NM_001006941.2:c.250T>C
(ALG3)
|
NP_001006942.1:p.Tyr84His
|
|
NM_005787.5:c.394T>C
(ALG3)
|
NP_005778.1:p.Tyr132His
|
|
NR_024533.1:n.325T>C
(ALG3)
|
|
|
NR_024534.1:n.388T>C
(ALG3)
|
|
|
XM_011512322.1:c.295T>C
(ALG3)
|
XP_011510624.1:p.Tyr99His
|
|
XM_011512323.1:c.274T>C
(ALG3)
|
XP_011510625.1:p.Tyr92His
|
|
XM_011512323.2:c.274T>C
(ALG3)
|
XP_011510625.1:p.Tyr92His
|
|
XM_024453296.1:c.172T>C
(ALG3)
|
XP_024309064.1:p.Tyr58His
|
|
NM_005787.6:c.394T>C
(ALG3)
MANE Select
|
NP_005778.1:p.Tyr132His
|
|