ENST00000397676.8:c.605+97G>T
(ALG3)
MANE Select
|
ENSP00000380793.3:n.605+97G>T
|
|
ENST00000397676.7:c.605+97G>T
(ALG3)
|
ENSP00000380793.3:n.605+97G>T
|
|
ENST00000411922.5:c.*181+97G>T
(ALG3)
|
ENSP00000394917.1:n.*181+97G>T
|
|
ENST00000414845.5:c.337+367G>T
(ALG3)
|
|
|
ENST00000423996.5:c.*370+97G>T
(ALG3)
|
ENSP00000407011.1:n.*370+97G>T
|
|
ENST00000444495.1:c.2106+100394C>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+100394C>A
|
|
ENST00000445626.6:c.461+97G>T
(ALG3)
|
ENSP00000402744.2:n.461+97G>T
|
|
ENST00000446569.1:c.315+97G>T
(ALG3)
|
|
|
ENST00000455059.5:c.485+97G>T
(ALG3)
|
ENSP00000397613.1:n.485+97G>T
|
|
ENST00000461415.5:n.675G>T
(ALG3)
|
|
|
ENST00000477959.1:n.145+97G>T
(ALG3)
|
|
|
ENST00000482048.1:n.691G>T
(ALG3)
|
|
|
ENST00000488976.5:n.587G>T
(ALG3)
|
|
|
NM_001006941.2:c.461+97G>T
(ALG3)
|
NP_001006942.1:n.461+97G>T
|
|
NM_005787.5:c.605+97G>T
(ALG3)
|
NP_005778.1:n.605+97G>T
|
|
NR_024533.1:n.536+97G>T
(ALG3)
|
|
|
NR_024534.1:n.599+97G>T
(ALG3)
|
|
|
XM_011512322.1:c.506+97G>T
(ALG3)
|
XP_011510624.1:n.506+97G>T
|
|
XM_011512323.1:c.485+97G>T
(ALG3)
|
XP_011510625.1:n.485+97G>T
|
|
XM_011512323.2:c.485+97G>T
(ALG3)
|
XP_011510625.1:n.485+97G>T
|
|
XM_024453296.1:c.383+97G>T
(ALG3)
|
XP_024309064.1:n.383+97G>T
|
|
NM_005787.6:c.605+97G>T
(ALG3)
MANE Select
|
NP_005778.1:n.605+97G>T
|
|