ENST00000324856.13:c.5337G=
MANE Select
|
ENSP00000320485.7:p.Glu1779=
|
|
ENST00000374152.7:c.4188G=
|
ENSP00000363267.2:p.Glu1396=
|
|
ENST00000430799.7:c.4185G=
|
ENSP00000390317.3:p.Glu1395=
|
|
ENST00000466382.2:c.754G=
|
|
|
ENST00000636219.1:c.4191G=
|
ENSP00000489842.1:p.Glu1397=
|
|
ENST00000637788.1:n.1137G=
|
|
|
ENST00000324856.11:c.5337G=
|
ENSP00000320485.7:p.Glu1779=
|
|
ENST00000374152.6:c.4188G=
|
ENSP00000363267.2:p.Glu1396=
|
|
ENST00000430799.6:c.2026G=
|
|
|
ENST00000457599.6:c.4686G=
|
ENSP00000387636.2:p.Glu1562=
|
|
ENST00000466382.1:c.754G=
|
|
|
ENST00000532781.1:c.835G=
|
|
|
NM_006015.4:c.5337G= , LRG_875t1:c.5337G=
|
NP_006006.3:p.Glu1779=
|
|
NM_139135.2:c.4686G=
|
NP_624361.1:p.Glu1562=
|
|
NM_006015.5:c.5337G=
|
NP_006006.3:p.Glu1779=
|
|
NM_139135.3:c.4686G=
|
NP_624361.1:p.Glu1562=
|
|
NM_006015.6:c.5337G=
MANE Select
|
NP_006006.3:p.Glu1779=
|
|
NM_139135.4:c.4686G=
|
NP_624361.1:p.Glu1562=
|
|