ENST00000324856.13:c.5264G>A
MANE Select
|
ENSP00000320485.7:p.Ser1755Asn
|
|
ENST00000374152.7:c.4115G>A
|
ENSP00000363267.2:p.Ser1372Asn
|
|
ENST00000430799.7:c.4112G>A
|
ENSP00000390317.3:p.Ser1371Asn
|
|
ENST00000466382.2:c.681G>A
|
|
|
ENST00000636219.1:c.4118G>A
|
ENSP00000489842.1:p.Ser1373Asn
|
|
ENST00000637788.1:n.1064G>A
|
|
|
ENST00000324856.11:c.5264G>A
|
ENSP00000320485.7:p.Ser1755Asn
|
|
ENST00000374152.6:c.4115G>A
|
ENSP00000363267.2:p.Ser1372Asn
|
|
ENST00000430799.6:c.1953G>A
|
|
|
ENST00000457599.6:c.4613G>A
|
ENSP00000387636.2:p.Ser1538Asn
|
|
ENST00000466382.1:c.681G>A
|
|
|
ENST00000532781.1:c.762G>A
|
|
|
NM_006015.4:c.5264G>A , LRG_875t1:c.5264G>A
|
NP_006006.3:p.Ser1755Asn
|
|
NM_139135.2:c.4613G>A
|
NP_624361.1:p.Ser1538Asn
|
|
NM_006015.5:c.5264G>A
|
NP_006006.3:p.Ser1755Asn
|
|
NM_139135.3:c.4613G>A
|
NP_624361.1:p.Ser1538Asn
|
|
NM_006015.6:c.5264G>A
MANE Select
|
NP_006006.3:p.Ser1755Asn
|
|
NM_139135.4:c.4613G>A
|
NP_624361.1:p.Ser1538Asn
|
|