ENST00000324856.13:c.5461G>C
MANE Select
|
ENSP00000320485.7:p.Asp1821His
|
|
ENST00000374152.7:c.4312G>C
|
ENSP00000363267.2:p.Asp1438His
|
|
ENST00000430799.7:c.4309G>C
|
ENSP00000390317.3:p.Asp1437His
|
|
ENST00000466382.2:c.878G>C
|
|
|
ENST00000636219.1:c.4315G>C
|
ENSP00000489842.1:p.Asp1439His
|
|
ENST00000637788.1:n.1261G>C
|
|
|
ENST00000324856.11:c.5461G>C
|
ENSP00000320485.7:p.Asp1821His
|
|
ENST00000374152.6:c.4312G>C
|
ENSP00000363267.2:p.Asp1438His
|
|
ENST00000430799.6:c.2150G>C
|
|
|
ENST00000457599.6:c.4810G>C
|
ENSP00000387636.2:p.Asp1604His
|
|
ENST00000466382.1:c.878G>C
|
|
|
ENST00000532781.1:c.959G>C
|
|
|
NM_006015.4:c.5461G>C , LRG_875t1:c.5461G>C
|
NP_006006.3:p.Asp1821His
|
|
NM_139135.2:c.4810G>C
|
NP_624361.1:p.Asp1604His
|
|
NM_006015.5:c.5461G>C
|
NP_006006.3:p.Asp1821His
|
|
NM_139135.3:c.4810G>C
|
NP_624361.1:p.Asp1604His
|
|
NM_006015.6:c.5461G>C
MANE Select
|
NP_006006.3:p.Asp1821His
|
|
NM_139135.4:c.4810G>C
|
NP_624361.1:p.Asp1604His
|
|