ENST00000521508.2:c.1223T>G
(ALG11)
MANE Select
|
ENSP00000430236.1:p.Met408Arg
|
|
ENST00000649340.2:c.1220T>G
(ALG11)
|
ENSP00000497184.2:p.Met407Arg
|
|
ENST00000649651.2:n.5527T>G
(ALG11)
|
|
|
ENST00000649708.2:c.275+9191T>G
(ALG11)
|
ENSP00000497459.2:n.275+9191T>G
|
|
ENST00000650049.2:c.*331T>G
(ALG11)
|
ENSP00000497398.2:n.*331T>G
|
|
ENST00000679359.1:c.*975T>G
(ALG11)
|
ENSP00000505579.1:n.*975T>G
|
|
ENST00000679495.1:n.44+15872T>G
(ALG11)
|
|
|
ENST00000679544.1:c.291T>G
(ALG11)
|
ENSP00000505560.1:p.Tyr97Ter
|
|
ENST00000680058.1:n.1126T>G
(ALG11)
|
|
|
ENST00000680793.1:n.2215T>G
(ALG11)
|
|
|
ENST00000680950.1:n.1350T>G
(ALG11)
|
|
|
ENST00000681047.1:c.*948T>G
(ALG11)
|
ENSP00000505034.1:n.*948T>G
|
|
ENST00000681053.1:c.992T>G
(ALG11)
|
ENSP00000505307.1:p.Met331Arg
|
|
ENST00000681145.1:c.*13T>G
(ALG11)
|
ENSP00000505163.1:n.*13T>G
|
|
ENST00000681226.1:n.411T>G
(ALG11)
|
|
|
ENST00000519151.1:n.4159T>G
(ALG11)
|
|
|
ENST00000521508.1:c.1223T>G
(ALG11)
|
ENSP00000430236.1:p.Met408Arg
|
|
ENST00000521776.2:c.-471T>G
(UTP14C)
MANE Select
|
ENSP00000428619.1:n.-471T>G
|
|
ENST00000523764.1:c.60T>G
(ALG11)
|
ENSP00000429497.1:p.Tyr20Ter
|
|
NM_001004127.2:c.1223T>G
(ALG11)
|
NP_001004127.2:p.Met408Arg
|
|
NM_021645.5:c.-471T>G
(UTP14C)
|
NP_067677.4:n.-471T>G
|
|
NR_036571.2:n.92T>G
(ALG11)
|
|
|
NM_001004127.3:c.1223T>G
(ALG11)
MANE Select
|
NP_001004127.2:p.Met408Arg
|
|
NM_021645.6:c.-471T>G
(UTP14C)
MANE Select
|
NP_067677.4:n.-471T>G
|
|
NR_036571.3:n.81T>G
(ALG11)
|
|
|