ENST00000397676.8:c.605+119C>T
(ALG3)
MANE Select
|
ENSP00000380793.3:n.605+119C>T
|
|
ENST00000397676.7:c.605+119C>T
(ALG3)
|
ENSP00000380793.3:n.605+119C>T
|
|
ENST00000411922.5:c.*181+119C>T
(ALG3)
|
ENSP00000394917.1:n.*181+119C>T
|
|
ENST00000414845.5:c.338-358C>T
(ALG3)
|
|
|
ENST00000423996.5:c.*370+119C>T
(ALG3)
|
ENSP00000407011.1:n.*370+119C>T
|
|
ENST00000444495.1:c.2106+100372G>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100372G>A
|
|
ENST00000445626.6:c.461+119C>T
(ALG3)
|
ENSP00000402744.2:n.461+119C>T
|
|
ENST00000446569.1:c.315+119C>T
(ALG3)
|
|
|
ENST00000455059.5:c.485+119C>T
(ALG3)
|
ENSP00000397613.1:n.485+119C>T
|
|
ENST00000461415.5:n.697C>T
(ALG3)
|
|
|
ENST00000477959.1:n.145+119C>T
(ALG3)
|
|
|
ENST00000482048.1:n.713C>T
(ALG3)
|
|
|
ENST00000488976.5:n.609C>T
(ALG3)
|
|
|
NM_001006941.2:c.461+119C>T
(ALG3)
|
NP_001006942.1:n.461+119C>T
|
|
NM_005787.5:c.605+119C>T
(ALG3)
|
NP_005778.1:n.605+119C>T
|
|
NR_024533.1:n.536+119C>T
(ALG3)
|
|
|
NR_024534.1:n.599+119C>T
(ALG3)
|
|
|
XM_011512322.1:c.506+119C>T
(ALG3)
|
XP_011510624.1:n.506+119C>T
|
|
XM_011512323.1:c.485+119C>T
(ALG3)
|
XP_011510625.1:n.485+119C>T
|
|
XM_011512323.2:c.485+119C>T
(ALG3)
|
XP_011510625.1:n.485+119C>T
|
|
XM_024453296.1:c.383+119C>T
(ALG3)
|
XP_024309064.1:n.383+119C>T
|
|
NM_005787.6:c.605+119C>T
(ALG3)
MANE Select
|
NP_005778.1:n.605+119C>T
|
|