ENST00000324856.13:c.5341G>A
MANE Select
|
ENSP00000320485.7:p.Val1781Ile
|
|
ENST00000374152.7:c.4192G>A
|
ENSP00000363267.2:p.Val1398Ile
|
|
ENST00000430799.7:c.4189G>A
|
ENSP00000390317.3:p.Val1397Ile
|
|
ENST00000466382.2:c.758G>A
|
|
|
ENST00000636219.1:c.4195G>A
|
ENSP00000489842.1:p.Val1399Ile
|
|
ENST00000637788.1:n.1141G>A
|
|
|
ENST00000324856.11:c.5341G>A
|
ENSP00000320485.7:p.Val1781Ile
|
|
ENST00000374152.6:c.4192G>A
|
ENSP00000363267.2:p.Val1398Ile
|
|
ENST00000430799.6:c.2030G>A
|
|
|
ENST00000457599.6:c.4690G>A
|
ENSP00000387636.2:p.Val1564Ile
|
|
ENST00000466382.1:c.758G>A
|
|
|
ENST00000532781.1:c.839G>A
|
|
|
NM_006015.4:c.5341G>A , LRG_875t1:c.5341G>A
|
NP_006006.3:p.Val1781Ile
|
|
NM_139135.2:c.4690G>A
|
NP_624361.1:p.Val1564Ile
|
|
NM_006015.5:c.5341G>A
|
NP_006006.3:p.Val1781Ile
|
|
NM_139135.3:c.4690G>A
|
NP_624361.1:p.Val1564Ile
|
|
NM_006015.6:c.5341G>A
MANE Select
|
NP_006006.3:p.Val1781Ile
|
|
NM_139135.4:c.4690G>A
|
NP_624361.1:p.Val1564Ile
|
|