ENST00000397676.8:c.580T>G
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Trp194Gly
|
|
ENST00000397676.7:c.580T>G
(ALG3)
|
ENSP00000380793.3:p.Trp194Gly
|
|
ENST00000411922.5:c.*156T>G
(ALG3)
|
ENSP00000394917.1:n.*156T>G
|
|
ENST00000414845.5:c.337+245T>G
(ALG3)
|
|
|
ENST00000423996.5:c.*345T>G
(ALG3)
|
ENSP00000407011.1:n.*345T>G
|
|
ENST00000444495.1:c.2106+100516A>C
(EIF2B5)
|
ENSP00000409142.1:n.2106+100516A>C
|
|
ENST00000445626.6:c.436T>G
(ALG3)
|
ENSP00000402744.2:p.Trp146Gly
|
|
ENST00000446569.1:c.290T>G
(ALG3)
|
|
|
ENST00000455059.5:c.460T>G
(ALG3)
|
ENSP00000397613.1:p.Trp154Gly
|
|
ENST00000461415.5:n.553T>G
(ALG3)
|
|
|
ENST00000477959.1:n.120T>G
(ALG3)
|
|
|
ENST00000482048.1:n.569T>G
(ALG3)
|
|
|
ENST00000488976.5:n.465T>G
(ALG3)
|
|
|
NM_001006941.2:c.436T>G
(ALG3)
|
NP_001006942.1:p.Trp146Gly
|
|
NM_005787.5:c.580T>G
(ALG3)
|
NP_005778.1:p.Trp194Gly
|
|
NR_024533.1:n.511T>G
(ALG3)
|
|
|
NR_024534.1:n.574T>G
(ALG3)
|
|
|
XM_011512322.1:c.481T>G
(ALG3)
|
XP_011510624.1:p.Trp161Gly
|
|
XM_011512323.1:c.460T>G
(ALG3)
|
XP_011510625.1:p.Trp154Gly
|
|
XM_011512323.2:c.460T>G
(ALG3)
|
XP_011510625.1:p.Trp154Gly
|
|
XM_024453296.1:c.358T>G
(ALG3)
|
XP_024309064.1:p.Trp120Gly
|
|
NM_005787.6:c.580T>G
(ALG3)
MANE Select
|
NP_005778.1:p.Trp194Gly
|
|