ENST00000698724.1:n.9G=
|
|
|
ENST00000698727.1:n.1801G=
|
|
|
ENST00000698728.1:n.2320G=
|
|
|
ENST00000698729.1:n.3866G=
|
|
|
ENST00000698730.1:n.3866G=
|
|
|
ENST00000698731.1:c.2600G=
|
ENSP00000513898.1:p.Gly867=
|
|
ENST00000698732.1:c.*1602G=
|
ENSP00000513899.1:n.*1602G=
|
|
ENST00000698733.1:c.*1928G=
|
ENSP00000513900.1:n.*1928G=
|
|
ENST00000698734.1:c.*265G=
|
ENSP00000513901.1:n.*265G=
|
|
ENST00000698735.1:n.2856G=
|
|
|
ENST00000698736.1:n.2856G=
|
|
|
ENST00000698737.1:n.2856G=
|
|
|
ENST00000698738.1:n.2856G=
|
|
|
ENST00000698739.1:n.2856G=
|
|
|
ENST00000372371.8:c.2741G=
MANE Select
|
ENSP00000361446.3:p.Gly914=
|
|
ENST00000372371.7:c.2741G=
|
ENSP00000361446.3:p.Gly914=
|
|
ENST00000472014.5:n.594G=
|
|
|
NM_007055.3:c.2741G=
|
NP_008986.2:p.Gly914=
|
|
NM_007055.4:c.2741G=
MANE Select
|
NP_008986.2:p.Gly914=
|
|