ENST00000698724.1:n.1825T>G
|
|
|
ENST00000698725.1:n.1578T>G
|
|
|
ENST00000698726.1:n.3138T>G
|
|
|
ENST00000698727.1:n.2871T>G
|
|
|
ENST00000698728.1:n.3487T>G
|
|
|
ENST00000698729.1:n.4935T>G
|
|
|
ENST00000698730.1:n.5033T>G
|
|
|
ENST00000698731.1:c.3767T>G
|
ENSP00000513898.1:p.Ile1256Ser
|
|
ENST00000698732.1:c.*2597T>G
|
ENSP00000513899.1:n.*2597T>G
|
|
ENST00000698733.1:c.*3095T>G
|
ENSP00000513900.1:n.*3095T>G
|
|
ENST00000698734.1:c.*2081T>G
|
ENSP00000513901.1:n.*2081T>G
|
|
ENST00000698735.1:n.4259T>G
|
|
|
ENST00000698736.1:n.4672T>G
|
|
|
ENST00000698737.1:n.4023T>G
|
|
|
ENST00000372371.8:c.3908T>G
MANE Select
|
ENSP00000361446.3:p.Ile1303Ser
|
|
ENST00000372371.7:c.3908T>G
|
ENSP00000361446.3:p.Ile1303Ser
|
|
ENST00000616246.4:c.356T>G
|
ENSP00000483738.1:p.Ile119Ser
|
|
NM_007055.3:c.3908T>G
|
NP_008986.2:p.Ile1303Ser
|
|
NM_007055.4:c.3908T>G
MANE Select
|
NP_008986.2:p.Ile1303Ser
|
|