ENST00000324856.13:c.5265T>C
MANE Select
|
ENSP00000320485.7:p.Ser1755=
|
|
ENST00000374152.7:c.4116T>C
|
ENSP00000363267.2:p.Ser1372=
|
|
ENST00000430799.7:c.4113T>C
|
ENSP00000390317.3:p.Ser1371=
|
|
ENST00000466382.2:c.682T>C
|
|
|
ENST00000636219.1:c.4119T>C
|
ENSP00000489842.1:p.Ser1373=
|
|
ENST00000637788.1:n.1065T>C
|
|
|
ENST00000324856.11:c.5265T>C
|
ENSP00000320485.7:p.Ser1755=
|
|
ENST00000374152.6:c.4116T>C
|
ENSP00000363267.2:p.Ser1372=
|
|
ENST00000430799.6:c.1954T>C
|
|
|
ENST00000457599.6:c.4614T>C
|
ENSP00000387636.2:p.Ser1538=
|
|
ENST00000466382.1:c.682T>C
|
|
|
ENST00000532781.1:c.763T>C
|
|
|
NM_006015.4:c.5265T>C , LRG_875t1:c.5265T>C
|
NP_006006.3:p.Ser1755=
|
|
NM_139135.2:c.4614T>C
|
NP_624361.1:p.Ser1538=
|
|
NM_006015.5:c.5265T>C
|
NP_006006.3:p.Ser1755=
|
|
NM_139135.3:c.4614T>C
|
NP_624361.1:p.Ser1538=
|
|
NM_006015.6:c.5265T>C
MANE Select
|
NP_006006.3:p.Ser1755=
|
|
NM_139135.4:c.4614T>C
|
NP_624361.1:p.Ser1538=
|
|