ENST00000397676.8:c.536T=
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Met179=
|
|
ENST00000397676.7:c.536T=
(ALG3)
|
ENSP00000380793.3:p.Met179=
|
|
ENST00000411922.5:c.*112T=
(ALG3)
|
ENSP00000394917.1:n.*112T=
|
|
ENST00000414845.5:c.337+201T=
(ALG3)
|
|
|
ENST00000423996.5:c.*301T=
(ALG3)
|
ENSP00000407011.1:n.*301T=
|
|
ENST00000444495.1:c.2106+100560A=
(EIF2B5)
|
ENSP00000409142.1:n.2106+100560A=
|
|
ENST00000445626.6:c.392T=
(ALG3)
|
ENSP00000402744.2:p.Met131=
|
|
ENST00000446569.1:c.246T=
(ALG3)
|
|
|
ENST00000455059.5:c.416T=
(ALG3)
|
ENSP00000397613.1:p.Met139=
|
|
ENST00000461415.5:n.509T=
(ALG3)
|
|
|
ENST00000477959.1:n.76T=
(ALG3)
|
|
|
ENST00000482048.1:n.525T=
(ALG3)
|
|
|
ENST00000488976.5:n.421T=
(ALG3)
|
|
|
NM_001006941.2:c.392T=
(ALG3)
|
NP_001006942.1:p.Met131=
|
|
NM_005787.5:c.536T=
(ALG3)
|
NP_005778.1:p.Met179=
|
|
NR_024533.1:n.467T=
(ALG3)
|
|
|
NR_024534.1:n.530T=
(ALG3)
|
|
|
XM_011512322.1:c.437T=
(ALG3)
|
XP_011510624.1:p.Met146=
|
|
XM_011512323.1:c.416T=
(ALG3)
|
XP_011510625.1:p.Met139=
|
|
XM_011512323.2:c.416T=
(ALG3)
|
XP_011510625.1:p.Met139=
|
|
XM_024453296.1:c.314T=
(ALG3)
|
XP_024309064.1:p.Met105=
|
|
NM_005787.6:c.536T=
(ALG3)
MANE Select
|
NP_005778.1:p.Met179=
|
|