ENST00000695651.1:n.960C>G
|
|
|
ENST00000695652.1:c.2489C>G
|
ENSP00000512083.1:p.Ala830Gly
|
|
ENST00000695653.1:c.521C>G
|
ENSP00000512084.1:p.Ala174Gly
|
|
ENST00000695654.1:c.1736C>G
|
ENSP00000512085.1:p.Ala579Gly
|
|
ENST00000695655.1:c.1553C>G
|
ENSP00000512086.1:n.1553C>G
|
|
ENST00000695692.1:n.1976C>G
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|
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ENST00000245907.11:c.2612C>G
MANE Select
|
ENSP00000245907.4:p.Ala871Gly
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|
ENST00000245907.10:c.2612C>G
|
ENSP00000245907.4:p.Ala871Gly
|
|
ENST00000594005.1:n.188C>G
|
|
|
NM_000064.3:c.2612C>G
|
NP_000055.2:p.Ala871Gly
|
|
NM_000064.4:c.2612C>G
MANE Select
|
NP_000055.2:p.Ala871Gly
|
|