ENST00000698724.1:n.1824A>G
|
|
|
ENST00000698725.1:n.1577A>G
|
|
|
ENST00000698726.1:n.3137A>G
|
|
|
ENST00000698727.1:n.2870A>G
|
|
|
ENST00000698728.1:n.3486A>G
|
|
|
ENST00000698729.1:n.4934A>G
|
|
|
ENST00000698730.1:n.5032A>G
|
|
|
ENST00000698731.1:c.3766A>G
|
ENSP00000513898.1:p.Ile1256Val
|
|
ENST00000698732.1:c.*2596A>G
|
ENSP00000513899.1:n.*2596A>G
|
|
ENST00000698733.1:c.*3094A>G
|
ENSP00000513900.1:n.*3094A>G
|
|
ENST00000698734.1:c.*2080A>G
|
ENSP00000513901.1:n.*2080A>G
|
|
ENST00000698735.1:n.4258A>G
|
|
|
ENST00000698736.1:n.4671A>G
|
|
|
ENST00000698737.1:n.4022A>G
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|
|
ENST00000372371.8:c.3907A>G
MANE Select
|
ENSP00000361446.3:p.Ile1303Val
|
|
ENST00000372371.7:c.3907A>G
|
ENSP00000361446.3:p.Ile1303Val
|
|
ENST00000616246.4:c.355A>G
|
ENSP00000483738.1:p.Ile119Val
|
|
NM_007055.3:c.3907A>G
|
NP_008986.2:p.Ile1303Val
|
|
NM_007055.4:c.3907A>G
MANE Select
|
NP_008986.2:p.Ile1303Val
|
|