ENST00000698724.1:n.1853G>T
|
|
|
ENST00000698725.1:n.1606G>T
|
|
|
ENST00000698726.1:n.3166G>T
|
|
|
ENST00000698727.1:n.2899G>T
|
|
|
ENST00000698728.1:n.3515G>T
|
|
|
ENST00000698729.1:n.4963G>T
|
|
|
ENST00000698730.1:n.5061G>T
|
|
|
ENST00000698731.1:c.3795G>T
|
ENSP00000513898.1:p.Lys1265Asn
|
|
ENST00000698732.1:c.*2625G>T
|
ENSP00000513899.1:n.*2625G>T
|
|
ENST00000698733.1:c.*3123G>T
|
ENSP00000513900.1:n.*3123G>T
|
|
ENST00000698734.1:c.*2109G>T
|
ENSP00000513901.1:n.*2109G>T
|
|
ENST00000698735.1:n.4287G>T
|
|
|
ENST00000698736.1:n.4700G>T
|
|
|
ENST00000698737.1:n.4051G>T
|
|
|
ENST00000372371.8:c.3936G>T
MANE Select
|
ENSP00000361446.3:p.Lys1312Asn
|
|
ENST00000372371.7:c.3936G>T
|
ENSP00000361446.3:p.Lys1312Asn
|
|
ENST00000616246.4:c.384G>T
|
ENSP00000483738.1:p.Lys128Asn
|
|
NM_007055.3:c.3936G>T
|
NP_008986.2:p.Lys1312Asn
|
|
NM_007055.4:c.3936G>T
MANE Select
|
NP_008986.2:p.Lys1312Asn
|
|