ENST00000698724.1:n.1862G>C
|
|
|
ENST00000698725.1:n.1615G>C
|
|
|
ENST00000698726.1:n.3175G>C
|
|
|
ENST00000698727.1:n.2908G>C
|
|
|
ENST00000698728.1:n.3524G>C
|
|
|
ENST00000698729.1:n.4972G>C
|
|
|
ENST00000698730.1:n.5070G>C
|
|
|
ENST00000698731.1:c.3804G>C
|
ENSP00000513898.1:p.Val1268=
|
|
ENST00000698732.1:c.*2634G>C
|
ENSP00000513899.1:n.*2634G>C
|
|
ENST00000698733.1:c.*3132G>C
|
ENSP00000513900.1:n.*3132G>C
|
|
ENST00000698734.1:c.*2118G>C
|
ENSP00000513901.1:n.*2118G>C
|
|
ENST00000698735.1:n.4296G>C
|
|
|
ENST00000698736.1:n.4709G>C
|
|
|
ENST00000698737.1:n.4060G>C
|
|
|
ENST00000372371.8:c.3945G>C
MANE Select
|
ENSP00000361446.3:p.Val1315=
|
|
ENST00000372371.7:c.3945G>C
|
ENSP00000361446.3:p.Val1315=
|
|
ENST00000616246.4:c.393G>C
|
ENSP00000483738.1:p.Val131=
|
|
NM_007055.3:c.3945G>C
|
NP_008986.2:p.Val1315=
|
|
NM_007055.4:c.3945G>C
MANE Select
|
NP_008986.2:p.Val1315=
|
|