ENST00000324856.13:c.5325G>C
MANE Select
|
ENSP00000320485.7:p.Glu1775Asp
|
|
ENST00000374152.7:c.4176G>C
|
ENSP00000363267.2:p.Glu1392Asp
|
|
ENST00000430799.7:c.4173G>C
|
ENSP00000390317.3:p.Glu1391Asp
|
|
ENST00000466382.2:c.742G>C
|
|
|
ENST00000636219.1:c.4179G>C
|
ENSP00000489842.1:p.Glu1393Asp
|
|
ENST00000637788.1:n.1125G>C
|
|
|
ENST00000324856.11:c.5325G>C
|
ENSP00000320485.7:p.Glu1775Asp
|
|
ENST00000374152.6:c.4176G>C
|
ENSP00000363267.2:p.Glu1392Asp
|
|
ENST00000430799.6:c.2014G>C
|
|
|
ENST00000457599.6:c.4674G>C
|
ENSP00000387636.2:p.Glu1558Asp
|
|
ENST00000466382.1:c.742G>C
|
|
|
ENST00000532781.1:c.823G>C
|
|
|
NM_006015.4:c.5325G>C , LRG_875t1:c.5325G>C
|
NP_006006.3:p.Glu1775Asp
|
|
NM_139135.2:c.4674G>C
|
NP_624361.1:p.Glu1558Asp
|
|
NM_006015.5:c.5325G>C
|
NP_006006.3:p.Glu1775Asp
|
|
NM_139135.3:c.4674G>C
|
NP_624361.1:p.Glu1558Asp
|
|
NM_006015.6:c.5325G>C
MANE Select
|
NP_006006.3:p.Glu1775Asp
|
|
NM_139135.4:c.4674G>C
|
NP_624361.1:p.Glu1558Asp
|
|