ENST00000698728.1:n.1235C>T
|
|
|
ENST00000698729.1:n.2781C>T
|
|
|
ENST00000698730.1:n.2781C>T
|
|
|
ENST00000698731.1:c.1515C>T
|
ENSP00000513898.1:p.Leu505=
|
|
ENST00000698732.1:c.*517C>T
|
ENSP00000513899.1:n.*517C>T
|
|
ENST00000698733.1:c.*843C>T
|
ENSP00000513900.1:n.*843C>T
|
|
ENST00000698734.1:c.1656C>T
|
ENSP00000513901.1:p.Leu552=
|
|
ENST00000698735.1:n.1771C>T
|
|
|
ENST00000698736.1:n.1771C>T
|
|
|
ENST00000698737.1:n.1771C>T
|
|
|
ENST00000698738.1:n.1771C>T
|
|
|
ENST00000698739.1:n.1771C>T
|
|
|
ENST00000372371.8:c.1656C>T
MANE Select
|
ENSP00000361446.3:p.Leu552=
|
|
ENST00000372371.7:c.1656C>T
|
ENSP00000361446.3:p.Leu552=
|
|
ENST00000473588.2:c.458C>T
|
|
|
NM_007055.3:c.1656C>T
|
NP_008986.2:p.Leu552=
|
|
NM_007055.4:c.1656C>T
MANE Select
|
NP_008986.2:p.Leu552=
|
|