ENST00000698728.1:n.1270C>G
|
|
|
ENST00000698729.1:n.2816C>G
|
|
|
ENST00000698730.1:n.2816C>G
|
|
|
ENST00000698731.1:c.1550C>G
|
ENSP00000513898.1:p.Ala517Gly
|
|
ENST00000698732.1:c.*552C>G
|
ENSP00000513899.1:n.*552C>G
|
|
ENST00000698733.1:c.*878C>G
|
ENSP00000513900.1:n.*878C>G
|
|
ENST00000698734.1:c.1691C>G
|
ENSP00000513901.1:p.Ala564Gly
|
|
ENST00000698735.1:n.1806C>G
|
|
|
ENST00000698736.1:n.1806C>G
|
|
|
ENST00000698737.1:n.1806C>G
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|
|
ENST00000698738.1:n.1806C>G
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|
|
ENST00000698739.1:n.1806C>G
|
|
|
ENST00000372371.8:c.1691C>G
MANE Select
|
ENSP00000361446.3:p.Ala564Gly
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|
ENST00000372371.7:c.1691C>G
|
ENSP00000361446.3:p.Ala564Gly
|
|
ENST00000473588.2:c.493C>G
|
|
|
NM_007055.3:c.1691C>G
|
NP_008986.2:p.Ala564Gly
|
|
NM_007055.4:c.1691C>G
MANE Select
|
NP_008986.2:p.Ala564Gly
|
|