ENST00000347132.10:c.776C>A
MANE Select
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ENSP00000262916.6:p.Ala259Asp
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ENST00000347132.9:c.776C>A
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ENSP00000262916.6:p.Ala259Asp
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ENST00000443478.3:c.462C>A
|
|
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ENST00000506017.1:n.95C>A
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ENST00000509682.6:c.776C>A
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ENSP00000423756.2:p.Ala259Asp
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NM_004700.3:c.776C>A
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NP_004691.2:p.Ala259Asp
|
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NM_172163.2:c.776C>A
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NP_751895.1:p.Ala259Asp
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XM_011542417.1:c.776C>A
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XP_011540719.1:p.Ala259Asp
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XM_011542418.1:c.776C>A
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XP_011540720.1:p.Ala259Asp
|
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XM_011542419.1:c.776C>A
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XP_011540721.1:p.Ala259Asp
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XM_011542420.1:c.776C>A
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XP_011540722.1:p.Ala259Asp
|
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XR_946798.1:n.782C>A
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|
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XR_946799.1:n.782C>A
|
|
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XR_946800.1:n.782C>A
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|
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XM_017002792.1:c.-242C>A
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XP_016858281.1:n.-242C>A
|
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NM_004700.4:c.776C>A
MANE Select
|
NP_004691.2:p.Ala259Asp
|
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NM_172163.3:c.776C>A
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NP_751895.1:p.Ala259Asp
|
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