ENST00000305046.13:c.213C>A
MANE Select
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ENSP00000306606.8:p.Ala71=
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ENST00000639454.1:c.213C>A
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ENSP00000491622.1:p.Ala71=
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ENST00000305046.12:c.213C>A
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ENSP00000306606.8:p.Ala71=
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ENST00000504498.1:n.267C>A
|
|
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ENST00000506651.5:c.93C>A
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ENSP00000425998.2:p.Ala31=
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ENST00000515694.4:n.2308C>A
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|
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ENST00000625860.2:c.93C>A
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ENSP00000486614.1:p.Ala31=
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ENST00000632775.1:n.776C>A
|
|
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NM_000668.5:c.213C>A
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NP_000659.2:p.Ala71=
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NM_001286650.1:c.93C>A
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NP_001273579.1:p.Ala31=
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NM_000668.6:c.213C>A
MANE Select
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NP_000659.2:p.Ala71=
|
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NM_001286650.2:c.93C>A
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NP_001273579.1:p.Ala31=
|
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