ENST00000698727.1:n.1668T>A
|
|
|
ENST00000698728.1:n.2187T>A
|
|
|
ENST00000698729.1:n.3733T>A
|
|
|
ENST00000698730.1:n.3733T>A
|
|
|
ENST00000698731.1:c.2467T>A
|
ENSP00000513898.1:p.Tyr823Asn
|
|
ENST00000698732.1:c.*1469T>A
|
ENSP00000513899.1:n.*1469T>A
|
|
ENST00000698733.1:c.*1795T>A
|
ENSP00000513900.1:n.*1795T>A
|
|
ENST00000698734.1:c.2608T>A
|
ENSP00000513901.1:p.Tyr870Asn
|
|
ENST00000698735.1:n.2723T>A
|
|
|
ENST00000698736.1:n.2723T>A
|
|
|
ENST00000698737.1:n.2723T>A
|
|
|
ENST00000698738.1:n.2723T>A
|
|
|
ENST00000698739.1:n.2723T>A
|
|
|
ENST00000372371.8:c.2608T>A
MANE Select
|
ENSP00000361446.3:p.Tyr870Asn
|
|
ENST00000372371.7:c.2608T>A
|
ENSP00000361446.3:p.Tyr870Asn
|
|
ENST00000472014.5:n.469+4727T>A
|
|
|
NM_007055.3:c.2608T>A
|
NP_008986.2:p.Tyr870Asn
|
|
NM_007055.4:c.2608T>A
MANE Select
|
NP_008986.2:p.Tyr870Asn
|
|