ENST00000397676.8:c.395A=
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Tyr132=
|
|
ENST00000397676.7:c.395A=
(ALG3)
|
ENSP00000380793.3:p.Tyr132=
|
|
ENST00000411922.5:c.295A=
(ALG3)
|
ENSP00000394917.1:p.Thr99=
|
|
ENST00000414845.5:c.288A=
(ALG3)
|
|
|
ENST00000423996.5:c.*160A=
(ALG3)
|
ENSP00000407011.1:n.*160A=
|
|
ENST00000444495.1:c.2106+100810T=
(EIF2B5)
|
ENSP00000409142.1:n.2106+100810T=
|
|
ENST00000445626.6:c.251A=
(ALG3)
|
ENSP00000402744.2:p.Tyr84=
|
|
ENST00000446569.1:c.155-159A=
(ALG3)
|
|
|
ENST00000455059.5:c.275A=
(ALG3)
|
ENSP00000397613.1:p.Tyr92=
|
|
ENST00000461415.5:n.368A=
(ALG3)
|
|
|
ENST00000482048.1:n.384A=
(ALG3)
|
|
|
ENST00000488976.5:n.280A=
(ALG3)
|
|
|
NM_001006941.2:c.251A=
(ALG3)
|
NP_001006942.1:p.Tyr84=
|
|
NM_005787.5:c.395A=
(ALG3)
|
NP_005778.1:p.Tyr132=
|
|
NR_024533.1:n.326A=
(ALG3)
|
|
|
NR_024534.1:n.389A=
(ALG3)
|
|
|
XM_011512322.1:c.296A=
(ALG3)
|
XP_011510624.1:p.Tyr99=
|
|
XM_011512323.1:c.275A=
(ALG3)
|
XP_011510625.1:p.Tyr92=
|
|
XM_011512323.2:c.275A=
(ALG3)
|
XP_011510625.1:p.Tyr92=
|
|
XM_024453296.1:c.173A=
(ALG3)
|
XP_024309064.1:p.Tyr58=
|
|
NM_005787.6:c.395A=
(ALG3)
MANE Select
|
NP_005778.1:p.Tyr132=
|
|