ENST00000698724.1:n.1835T>C
|
|
|
ENST00000698725.1:n.1588T>C
|
|
|
ENST00000698726.1:n.3148T>C
|
|
|
ENST00000698727.1:n.2881T>C
|
|
|
ENST00000698728.1:n.3497T>C
|
|
|
ENST00000698729.1:n.4945T>C
|
|
|
ENST00000698730.1:n.5043T>C
|
|
|
ENST00000698731.1:c.3777T>C
|
ENSP00000513898.1:p.Phe1259=
|
|
ENST00000698732.1:c.*2607T>C
|
ENSP00000513899.1:n.*2607T>C
|
|
ENST00000698733.1:c.*3105T>C
|
ENSP00000513900.1:n.*3105T>C
|
|
ENST00000698734.1:c.*2091T>C
|
ENSP00000513901.1:n.*2091T>C
|
|
ENST00000698735.1:n.4269T>C
|
|
|
ENST00000698736.1:n.4682T>C
|
|
|
ENST00000698737.1:n.4033T>C
|
|
|
ENST00000372371.8:c.3918T>C
MANE Select
|
ENSP00000361446.3:p.Phe1306=
|
|
ENST00000372371.7:c.3918T>C
|
ENSP00000361446.3:p.Phe1306=
|
|
ENST00000616246.4:c.366T>C
|
ENSP00000483738.1:p.Phe122=
|
|
NM_007055.3:c.3918T>C
|
NP_008986.2:p.Phe1306=
|
|
NM_007055.4:c.3918T>C
MANE Select
|
NP_008986.2:p.Phe1306=
|
|