ENST00000397676.8:c.525C>T
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Asp175=
|
|
ENST00000397676.7:c.525C>T
(ALG3)
|
ENSP00000380793.3:p.Asp175=
|
|
ENST00000411922.5:c.*101C>T
(ALG3)
|
ENSP00000394917.1:n.*101C>T
|
|
ENST00000414845.5:c.337+190C>T
(ALG3)
|
|
|
ENST00000423996.5:c.*290C>T
(ALG3)
|
ENSP00000407011.1:n.*290C>T
|
|
ENST00000444495.1:c.2106+100571G>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100571G>A
|
|
ENST00000445626.6:c.381C>T
(ALG3)
|
ENSP00000402744.2:p.Asp127=
|
|
ENST00000446569.1:c.235C>T
(ALG3)
|
|
|
ENST00000455059.5:c.405C>T
(ALG3)
|
ENSP00000397613.1:p.Asp135=
|
|
ENST00000461415.5:n.498C>T
(ALG3)
|
|
|
ENST00000477959.1:n.65C>T
(ALG3)
|
|
|
ENST00000482048.1:n.514C>T
(ALG3)
|
|
|
ENST00000488976.5:n.410C>T
(ALG3)
|
|
|
NM_001006941.2:c.381C>T
(ALG3)
|
NP_001006942.1:p.Asp127=
|
|
NM_005787.5:c.525C>T
(ALG3)
|
NP_005778.1:p.Asp175=
|
|
NR_024533.1:n.456C>T
(ALG3)
|
|
|
NR_024534.1:n.519C>T
(ALG3)
|
|
|
XM_011512322.1:c.426C>T
(ALG3)
|
XP_011510624.1:p.Asp142=
|
|
XM_011512323.1:c.405C>T
(ALG3)
|
XP_011510625.1:p.Asp135=
|
|
XM_011512323.2:c.405C>T
(ALG3)
|
XP_011510625.1:p.Asp135=
|
|
XM_024453296.1:c.303C>T
(ALG3)
|
XP_024309064.1:p.Asp101=
|
|
NM_005787.6:c.525C>T
(ALG3)
MANE Select
|
NP_005778.1:p.Asp175=
|
|