ENST00000698724.1:n.1832G>C
|
|
|
ENST00000698725.1:n.1585G>C
|
|
|
ENST00000698726.1:n.3145G>C
|
|
|
ENST00000698727.1:n.2878G>C
|
|
|
ENST00000698728.1:n.3494G>C
|
|
|
ENST00000698729.1:n.4942G>C
|
|
|
ENST00000698730.1:n.5040G>C
|
|
|
ENST00000698731.1:c.3774G>C
|
ENSP00000513898.1:p.Arg1258Ser
|
|
ENST00000698732.1:c.*2604G>C
|
ENSP00000513899.1:n.*2604G>C
|
|
ENST00000698733.1:c.*3102G>C
|
ENSP00000513900.1:n.*3102G>C
|
|
ENST00000698734.1:c.*2088G>C
|
ENSP00000513901.1:n.*2088G>C
|
|
ENST00000698735.1:n.4266G>C
|
|
|
ENST00000698736.1:n.4679G>C
|
|
|
ENST00000698737.1:n.4030G>C
|
|
|
ENST00000372371.8:c.3915G>C
MANE Select
|
ENSP00000361446.3:p.Arg1305Ser
|
|
ENST00000372371.7:c.3915G>C
|
ENSP00000361446.3:p.Arg1305Ser
|
|
ENST00000616246.4:c.363G>C
|
ENSP00000483738.1:p.Arg121Ser
|
|
NM_007055.3:c.3915G>C
|
NP_008986.2:p.Arg1305Ser
|
|
NM_007055.4:c.3915G>C
MANE Select
|
NP_008986.2:p.Arg1305Ser
|
|