ENST00000698727.1:n.1672T>C
|
|
|
ENST00000698728.1:n.2191T>C
|
|
|
ENST00000698729.1:n.3737T>C
|
|
|
ENST00000698730.1:n.3737T>C
|
|
|
ENST00000698731.1:c.2471T>C
|
ENSP00000513898.1:p.Met824Thr
|
|
ENST00000698732.1:c.*1473T>C
|
ENSP00000513899.1:n.*1473T>C
|
|
ENST00000698733.1:c.*1799T>C
|
ENSP00000513900.1:n.*1799T>C
|
|
ENST00000698734.1:c.2612T>C
|
ENSP00000513901.1:p.Met871Thr
|
|
ENST00000698735.1:n.2727T>C
|
|
|
ENST00000698736.1:n.2727T>C
|
|
|
ENST00000698737.1:n.2727T>C
|
|
|
ENST00000698738.1:n.2727T>C
|
|
|
ENST00000698739.1:n.2727T>C
|
|
|
ENST00000372371.8:c.2612T>C
MANE Select
|
ENSP00000361446.3:p.Met871Thr
|
|
ENST00000372371.7:c.2612T>C
|
ENSP00000361446.3:p.Met871Thr
|
|
ENST00000472014.5:n.469+4731T>C
|
|
|
NM_007055.3:c.2612T>C
|
NP_008986.2:p.Met871Thr
|
|
NM_007055.4:c.2612T>C
MANE Select
|
NP_008986.2:p.Met871Thr
|
|