ENST00000698724.1:n.1905G>A
|
|
|
ENST00000698725.1:n.1658G>A
|
|
|
ENST00000698726.1:n.3218G>A
|
|
|
ENST00000698727.1:n.2951G>A
|
|
|
ENST00000698728.1:n.3567G>A
|
|
|
ENST00000698729.1:n.5015G>A
|
|
|
ENST00000698730.1:n.5113G>A
|
|
|
ENST00000698731.1:c.3847G>A
|
ENSP00000513898.1:p.Asp1283Asn
|
|
ENST00000698732.1:c.*2677G>A
|
ENSP00000513899.1:n.*2677G>A
|
|
ENST00000698733.1:c.*3175G>A
|
ENSP00000513900.1:n.*3175G>A
|
|
ENST00000698734.1:c.*2161G>A
|
ENSP00000513901.1:n.*2161G>A
|
|
ENST00000698735.1:n.4339G>A
|
|
|
ENST00000698736.1:n.4752G>A
|
|
|
ENST00000698737.1:n.4103G>A
|
|
|
ENST00000372371.8:c.3988G>A
MANE Select
|
ENSP00000361446.3:p.Asp1330Asn
|
|
ENST00000372371.7:c.3988G>A
|
ENSP00000361446.3:p.Asp1330Asn
|
|
ENST00000616246.4:c.436G>A
|
ENSP00000483738.1:p.Asp146Asn
|
|
NM_007055.3:c.3988G>A
|
NP_008986.2:p.Asp1330Asn
|
|
NM_007055.4:c.3988G>A
MANE Select
|
NP_008986.2:p.Asp1330Asn
|
|