ENST00000336906.6:c.416C>A
MANE Select
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ENSP00000338082.4:p.Ala139Asp
|
|
ENST00000380252.6:c.251C>A
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ENSP00000369602.2:p.Ala84Asp
|
|
ENST00000642908.1:c.315+987C>A
|
ENSP00000495346.1:n.315+987C>A
|
|
ENST00000647543.1:c.378+38C>A
|
ENSP00000496470.1:n.378+38C>A
|
|
ENST00000336906.4:c.416C>A
|
ENSP00000338082.4:p.Ala139Asp
|
|
ENST00000380252.5:c.386C>A
|
ENSP00000369602.1:p.Ala129Asp
|
|
ENST00000380259.6:c.416C>A
|
ENSP00000369609.2:p.Ala139Asp
|
|
ENST00000620888.4:c.315+987C>A
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ENSP00000479637.1:n.315+987C>A
|
|
NM_000184.2:c.416C>A
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NP_000175.1:p.Ala139Asp
|
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NM_000184.3:c.416C>A
MANE Select
|
NP_000175.1:p.Ala139Asp
|
|