ENST00000698724.1:n.1860G=
|
|
|
ENST00000698725.1:n.1613G=
|
|
|
ENST00000698726.1:n.3173G=
|
|
|
ENST00000698727.1:n.2906G=
|
|
|
ENST00000698728.1:n.3522G=
|
|
|
ENST00000698729.1:n.4970G=
|
|
|
ENST00000698730.1:n.5068G=
|
|
|
ENST00000698731.1:c.3802G=
|
ENSP00000513898.1:p.Val1268=
|
|
ENST00000698732.1:c.*2632G=
|
ENSP00000513899.1:n.*2632G=
|
|
ENST00000698733.1:c.*3130G=
|
ENSP00000513900.1:n.*3130G=
|
|
ENST00000698734.1:c.*2116G=
|
ENSP00000513901.1:n.*2116G=
|
|
ENST00000698735.1:n.4294G=
|
|
|
ENST00000698736.1:n.4707G=
|
|
|
ENST00000698737.1:n.4058G=
|
|
|
ENST00000372371.8:c.3943G=
MANE Select
|
ENSP00000361446.3:p.Val1315=
|
|
ENST00000372371.7:c.3943G=
|
ENSP00000361446.3:p.Val1315=
|
|
ENST00000616246.4:c.391G=
|
ENSP00000483738.1:p.Val131=
|
|
NM_007055.3:c.3943G=
|
NP_008986.2:p.Val1315=
|
|
NM_007055.4:c.3943G=
MANE Select
|
NP_008986.2:p.Val1315=
|
|