ENST00000698728.1:n.1225C>T
|
|
|
ENST00000698729.1:n.2771C>T
|
|
|
ENST00000698730.1:n.2771C>T
|
|
|
ENST00000698731.1:c.1505C>T
|
ENSP00000513898.1:p.Ala502Val
|
|
ENST00000698732.1:c.*507C>T
|
ENSP00000513899.1:n.*507C>T
|
|
ENST00000698733.1:c.*833C>T
|
ENSP00000513900.1:n.*833C>T
|
|
ENST00000698734.1:c.1646C>T
|
ENSP00000513901.1:p.Ala549Val
|
|
ENST00000698735.1:n.1761C>T
|
|
|
ENST00000698736.1:n.1761C>T
|
|
|
ENST00000698737.1:n.1761C>T
|
|
|
ENST00000698738.1:n.1761C>T
|
|
|
ENST00000698739.1:n.1761C>T
|
|
|
ENST00000372371.8:c.1646C>T
MANE Select
|
ENSP00000361446.3:p.Ala549Val
|
|
ENST00000372371.7:c.1646C>T
|
ENSP00000361446.3:p.Ala549Val
|
|
ENST00000473588.2:c.448C>T
|
|
|
NM_007055.3:c.1646C>T
|
NP_008986.2:p.Ala549Val
|
|
NM_007055.4:c.1646C>T
MANE Select
|
NP_008986.2:p.Ala549Val
|
|