|
NM_005787.6:c.696C>T
(ALG3)
MANE Select
|
NP_005778.1:p.Leu232=
|
|
ENST00000397676.8:c.696C>T
(ALG3)
MANE Select
|
ENSP00000380793.3:p.Leu232=
|
|
NM_001006941.2:c.552C>T
(ALG3)
|
NP_001006942.1:p.Leu184=
|
|
NM_005787.5:c.696C>T
(ALG3)
|
NP_005778.1:p.Leu232=
|
|
NR_024533.1:n.627C>T
(ALG3)
|
|
|
NR_024534.1:n.690C>T
(ALG3)
|
|
|
ENST00000397676.7:c.696C>T
(ALG3)
|
ENSP00000380793.3:p.Leu232=
|
|
ENST00000411922.5:c.*272C>T
(ALG3)
|
ENSP00000394917.1:n.*272C>T
|
|
ENST00000414845.5:c.428C>T
(ALG3)
|
|
|
ENST00000423996.5:c.*461C>T
(ALG3)
|
ENSP00000407011.1:n.*461C>T
|
|
ENST00000444495.1:c.2106+99924G>A
(EIF2B5)
|
ENSP00000409142.1:n.2106+99924G>A
|
|
ENST00000445626.6:c.552C>T
(ALG3)
|
ENSP00000402744.2:p.Leu184=
|
|
ENST00000446569.1:c.406C>T
(ALG3)
|
|
|
ENST00000455059.5:c.576C>T
(ALG3)
|
ENSP00000397613.1:p.Leu192=
|
|
ENST00000462735.6:n.391C>T
(ALG3)
|
|
|
ENST00000477959.1:n.236C>T
(ALG3)
|
|
|
XM_011512322.1:c.597C>T
(ALG3)
|
XP_011510624.1:p.Leu199=
|
|
XM_011512323.1:c.576C>T
(ALG3)
|
XP_011510625.1:p.Leu192=
|
|
XM_011512323.2:c.576C>T
(ALG3)
|
XP_011510625.1:p.Leu192=
|
|
XM_024453296.1:c.474C>T
(ALG3)
|
XP_024309064.1:p.Leu158=
|
