ENST00000698724.1:n.1847G>T
|
|
|
ENST00000698725.1:n.1600G>T
|
|
|
ENST00000698726.1:n.3160G>T
|
|
|
ENST00000698727.1:n.2893G>T
|
|
|
ENST00000698728.1:n.3509G>T
|
|
|
ENST00000698729.1:n.4957G>T
|
|
|
ENST00000698730.1:n.5055G>T
|
|
|
ENST00000698731.1:c.3789G>T
|
ENSP00000513898.1:p.Lys1263Asn
|
|
ENST00000698732.1:c.*2619G>T
|
ENSP00000513899.1:n.*2619G>T
|
|
ENST00000698733.1:c.*3117G>T
|
ENSP00000513900.1:n.*3117G>T
|
|
ENST00000698734.1:c.*2103G>T
|
ENSP00000513901.1:n.*2103G>T
|
|
ENST00000698735.1:n.4281G>T
|
|
|
ENST00000698736.1:n.4694G>T
|
|
|
ENST00000698737.1:n.4045G>T
|
|
|
ENST00000372371.8:c.3930G>T
MANE Select
|
ENSP00000361446.3:p.Lys1310Asn
|
|
ENST00000372371.7:c.3930G>T
|
ENSP00000361446.3:p.Lys1310Asn
|
|
ENST00000616246.4:c.378G>T
|
ENSP00000483738.1:p.Lys126Asn
|
|
NM_007055.3:c.3930G>T
|
NP_008986.2:p.Lys1310Asn
|
|
NM_007055.4:c.3930G>T
MANE Select
|
NP_008986.2:p.Lys1310Asn
|
|