ENST00000324856.13:c.5335G>C
MANE Select
|
ENSP00000320485.7:p.Glu1779Gln
|
|
ENST00000374152.7:c.4186G>C
|
ENSP00000363267.2:p.Glu1396Gln
|
|
ENST00000430799.7:c.4183G>C
|
ENSP00000390317.3:p.Glu1395Gln
|
|
ENST00000466382.2:c.752G>C
|
|
|
ENST00000636219.1:c.4189G>C
|
ENSP00000489842.1:p.Glu1397Gln
|
|
ENST00000637788.1:n.1135G>C
|
|
|
ENST00000324856.11:c.5335G>C
|
ENSP00000320485.7:p.Glu1779Gln
|
|
ENST00000374152.6:c.4186G>C
|
ENSP00000363267.2:p.Glu1396Gln
|
|
ENST00000430799.6:c.2024G>C
|
|
|
ENST00000457599.6:c.4684G>C
|
ENSP00000387636.2:p.Glu1562Gln
|
|
ENST00000466382.1:c.752G>C
|
|
|
ENST00000532781.1:c.833G>C
|
|
|
NM_006015.4:c.5335G>C , LRG_875t1:c.5335G>C
|
NP_006006.3:p.Glu1779Gln
|
|
NM_139135.2:c.4684G>C
|
NP_624361.1:p.Glu1562Gln
|
|
NM_006015.5:c.5335G>C
|
NP_006006.3:p.Glu1779Gln
|
|
NM_139135.3:c.4684G>C
|
NP_624361.1:p.Glu1562Gln
|
|
NM_006015.6:c.5335G>C
MANE Select
|
NP_006006.3:p.Glu1779Gln
|
|
NM_139135.4:c.4684G>C
|
NP_624361.1:p.Glu1562Gln
|
|