ENST00000698727.1:n.1381G>T
|
|
|
ENST00000698728.1:n.1900G>T
|
|
|
ENST00000698729.1:n.3446G>T
|
|
|
ENST00000698730.1:n.3446G>T
|
|
|
ENST00000698731.1:c.2180G>T
|
ENSP00000513898.1:p.Ser727Ile
|
|
ENST00000698732.1:c.*1182G>T
|
ENSP00000513899.1:n.*1182G>T
|
|
ENST00000698733.1:c.*1508G>T
|
ENSP00000513900.1:n.*1508G>T
|
|
ENST00000698734.1:c.2321G>T
|
ENSP00000513901.1:p.Ser774Ile
|
|
ENST00000698735.1:n.2436G>T
|
|
|
ENST00000698736.1:n.2436G>T
|
|
|
ENST00000698737.1:n.2436G>T
|
|
|
ENST00000698738.1:n.2436G>T
|
|
|
ENST00000698739.1:n.2436G>T
|
|
|
ENST00000372371.8:c.2321G>T
MANE Select
|
ENSP00000361446.3:p.Ser774Ile
|
|
ENST00000372371.7:c.2321G>T
|
ENSP00000361446.3:p.Ser774Ile
|
|
ENST00000472014.5:n.469+2481G>T
|
|
|
ENST00000473588.2:c.984G>T
|
|
|
NM_007055.3:c.2321G>T
|
NP_008986.2:p.Ser774Ile
|
|
NM_007055.4:c.2321G>T
MANE Select
|
NP_008986.2:p.Ser774Ile
|
|