ENST00000324856.13:c.5282G>T
MANE Select
|
ENSP00000320485.7:p.Gly1761Val
|
|
ENST00000374152.7:c.4133G>T
|
ENSP00000363267.2:p.Gly1378Val
|
|
ENST00000430799.7:c.4130G>T
|
ENSP00000390317.3:p.Gly1377Val
|
|
ENST00000466382.2:c.699G>T
|
|
|
ENST00000636219.1:c.4136G>T
|
ENSP00000489842.1:p.Gly1379Val
|
|
ENST00000637788.1:n.1082G>T
|
|
|
ENST00000324856.11:c.5282G>T
|
ENSP00000320485.7:p.Gly1761Val
|
|
ENST00000374152.6:c.4133G>T
|
ENSP00000363267.2:p.Gly1378Val
|
|
ENST00000430799.6:c.1971G>T
|
|
|
ENST00000457599.6:c.4631G>T
|
ENSP00000387636.2:p.Gly1544Val
|
|
ENST00000466382.1:c.699G>T
|
|
|
ENST00000532781.1:c.780G>T
|
|
|
NM_006015.4:c.5282G>T , LRG_875t1:c.5282G>T
|
NP_006006.3:p.Gly1761Val
|
|
NM_139135.2:c.4631G>T
|
NP_624361.1:p.Gly1544Val
|
|
NM_006015.5:c.5282G>T
|
NP_006006.3:p.Gly1761Val
|
|
NM_139135.3:c.4631G>T
|
NP_624361.1:p.Gly1544Val
|
|
NM_006015.6:c.5282G>T
MANE Select
|
NP_006006.3:p.Gly1761Val
|
|
NM_139135.4:c.4631G>T
|
NP_624361.1:p.Gly1544Val
|
|