ENST00000698728.1:n.1255T>A
|
|
|
ENST00000698729.1:n.2801T>A
|
|
|
ENST00000698730.1:n.2801T>A
|
|
|
ENST00000698731.1:c.1535T>A
|
ENSP00000513898.1:p.Phe512Tyr
|
|
ENST00000698732.1:c.*537T>A
|
ENSP00000513899.1:n.*537T>A
|
|
ENST00000698733.1:c.*863T>A
|
ENSP00000513900.1:n.*863T>A
|
|
ENST00000698734.1:c.1676T>A
|
ENSP00000513901.1:p.Phe559Tyr
|
|
ENST00000698735.1:n.1791T>A
|
|
|
ENST00000698736.1:n.1791T>A
|
|
|
ENST00000698737.1:n.1791T>A
|
|
|
ENST00000698738.1:n.1791T>A
|
|
|
ENST00000698739.1:n.1791T>A
|
|
|
ENST00000372371.8:c.1676T>A
MANE Select
|
ENSP00000361446.3:p.Phe559Tyr
|
|
ENST00000372371.7:c.1676T>A
|
ENSP00000361446.3:p.Phe559Tyr
|
|
ENST00000473588.2:c.478T>A
|
|
|
NM_007055.3:c.1676T>A
|
NP_008986.2:p.Phe559Tyr
|
|
NM_007055.4:c.1676T>A
MANE Select
|
NP_008986.2:p.Phe559Tyr
|
|