ENST00000324856.13:c.5258T>C
MANE Select
|
ENSP00000320485.7:p.Val1753Ala
|
|
ENST00000374152.7:c.4109T>C
|
ENSP00000363267.2:p.Val1370Ala
|
|
ENST00000430799.7:c.4106T>C
|
ENSP00000390317.3:p.Val1369Ala
|
|
ENST00000466382.2:c.675T>C
|
|
|
ENST00000636219.1:c.4112T>C
|
ENSP00000489842.1:p.Val1371Ala
|
|
ENST00000637788.1:n.1058T>C
|
|
|
ENST00000324856.11:c.5258T>C
|
ENSP00000320485.7:p.Val1753Ala
|
|
ENST00000374152.6:c.4109T>C
|
ENSP00000363267.2:p.Val1370Ala
|
|
ENST00000430799.6:c.1947T>C
|
|
|
ENST00000457599.6:c.4607T>C
|
ENSP00000387636.2:p.Val1536Ala
|
|
ENST00000466382.1:c.675T>C
|
|
|
ENST00000532781.1:c.756T>C
|
|
|
NM_006015.4:c.5258T>C , LRG_875t1:c.5258T>C
|
NP_006006.3:p.Val1753Ala
|
|
NM_139135.2:c.4607T>C
|
NP_624361.1:p.Val1536Ala
|
|
NM_006015.5:c.5258T>C
|
NP_006006.3:p.Val1753Ala
|
|
NM_139135.3:c.4607T>C
|
NP_624361.1:p.Val1536Ala
|
|
NM_006015.6:c.5258T>C
MANE Select
|
NP_006006.3:p.Val1753Ala
|
|
NM_139135.4:c.4607T>C
|
NP_624361.1:p.Val1536Ala
|
|