ENST00000324856.13:c.1358C>A
MANE Select
|
ENSP00000320485.7:p.Pro453His
|
|
ENST00000374152.7:c.209C>A
|
ENSP00000363267.2:p.Pro70His
|
|
ENST00000430799.7:c.209C>A
|
ENSP00000390317.3:p.Pro70His
|
|
ENST00000636219.1:c.215C>A
|
ENSP00000489842.1:p.Pro72His
|
|
ENST00000637465.1:c.209C>A
|
ENSP00000490650.1:p.Pro70His
|
|
ENST00000324856.11:c.1358C>A
|
ENSP00000320485.7:p.Pro453His
|
|
ENST00000374152.6:c.209C>A
|
ENSP00000363267.2:p.Pro70His
|
|
ENST00000457599.6:c.1358C>A
|
ENSP00000387636.2:p.Pro453His
|
|
ENST00000524572.1:c.209C>A
|
ENSP00000432473.1:p.Pro70His
|
|
ENST00000615191.4:c.209C>A
|
ENSP00000478955.1:p.Pro70His
|
|
NM_006015.4:c.1358C>A , LRG_875t1:c.1358C>A
|
NP_006006.3:p.Pro453His
|
|
NM_139135.2:c.1358C>A
|
NP_624361.1:p.Pro453His
|
|
NM_006015.5:c.1358C>A
|
NP_006006.3:p.Pro453His
|
|
NM_139135.3:c.1358C>A
|
NP_624361.1:p.Pro453His
|
|
NM_006015.6:c.1358C>A
MANE Select
|
NP_006006.3:p.Pro453His
|
|
NM_139135.4:c.1358C>A
|
NP_624361.1:p.Pro453His
|
|