ENST00000695651.1:n.1089C>G
|
|
|
ENST00000695652.1:c.2618C>G
|
ENSP00000512083.1:p.Ala873Gly
|
|
ENST00000695653.1:c.650C>G
|
ENSP00000512084.1:p.Ala217Gly
|
|
ENST00000695654.1:c.1865C>G
|
ENSP00000512085.1:p.Ala622Gly
|
|
ENST00000695655.1:c.1682C>G
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ENSP00000512086.1:n.1682C>G
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ENST00000695692.1:n.2105C>G
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ENST00000245907.11:c.2741C>G
MANE Select
|
ENSP00000245907.4:p.Ala914Gly
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|
ENST00000245907.10:c.2741C>G
|
ENSP00000245907.4:p.Ala914Gly
|
|
ENST00000594005.1:n.317C>G
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|
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NM_000064.3:c.2741C>G
|
NP_000055.2:p.Ala914Gly
|
|
NM_000064.4:c.2741C>G
MANE Select
|
NP_000055.2:p.Ala914Gly
|
|