ENST00000324856.13:c.433C>G
MANE Select
|
ENSP00000320485.7:p.Pro145Ala
|
|
ENST00000430799.7:c.-13+3219C>G
|
ENSP00000390317.3:n.-13+3219C>G
|
|
ENST00000637465.1:c.-13+736C>G
|
ENSP00000490650.1:n.-13+736C>G
|
|
ENST00000324856.11:c.433C>G
|
ENSP00000320485.7:p.Pro145Ala
|
|
ENST00000457599.6:c.433C>G
|
ENSP00000387636.2:p.Pro145Ala
|
|
NM_006015.4:c.433C>G , LRG_875t1:c.433C>G
|
NP_006006.3:p.Pro145Ala
|
|
NM_139135.2:c.433C>G
|
NP_624361.1:p.Pro145Ala
|
|
NM_006015.5:c.433C>G
|
NP_006006.3:p.Pro145Ala
|
|
NM_139135.3:c.433C>G
|
NP_624361.1:p.Pro145Ala
|
|
NM_006015.6:c.433C>G
MANE Select
|
NP_006006.3:p.Pro145Ala
|
|
NM_139135.4:c.433C>G
|
NP_624361.1:p.Pro145Ala
|
|