ENST00000695651.1:n.2889C>G
|
|
|
ENST00000695653.1:c.2450C>G
|
ENSP00000512084.1:p.Ala817Gly
|
|
ENST00000695654.1:c.3566C>G
|
ENSP00000512085.1:p.Ala1189Gly
|
|
ENST00000695689.1:c.512C>G
|
ENSP00000512101.1:n.512C>G
|
|
ENST00000695690.1:n.1606C>G
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|
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ENST00000695691.1:n.1402C>G
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|
|
ENST00000245907.11:c.4541C>G
MANE Select
|
ENSP00000245907.4:p.Ala1514Gly
|
|
ENST00000245907.10:c.4541C>G
|
ENSP00000245907.4:p.Ala1514Gly
|
|
ENST00000599668.1:n.136C>G
|
|
|
ENST00000599899.5:n.1500C>G
|
|
|
ENST00000601008.1:c.242-1454C>G
|
ENSP00000471384.1:n.242-1454C>G
|
|
NM_000064.3:c.4541C>G
|
NP_000055.2:p.Ala1514Gly
|
|
NM_000064.4:c.4541C>G
MANE Select
|
NP_000055.2:p.Ala1514Gly
|
|