ENST00000426263.10:c.926C>T
MANE Select
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ENSP00000416293.2:p.Ala309Val
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ENST00000674545.1:n.244C>T
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|
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ENST00000674765.1:c.926C>T
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ENSP00000501811.1:p.Ala309Val
|
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ENST00000675112.1:n.1227C>T
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|
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ENST00000676254.1:n.1375C>T
|
|
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ENST00000426263.7:c.926C>T
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ENSP00000416293.2:p.Ala309Val
|
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ENST00000439722.2:c.805C>T
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ENSP00000395521.2:n.805C>T
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ENST00000475162.3:c.415+1370C>T
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|
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ENST00000630287.2:c.*241C>T
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ENSP00000486694.1:n.*241C>T
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NM_006516.2:c.926C>T
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NP_006507.2:p.Ala309Val
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NM_006516.3:c.926C>T
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NP_006507.2:p.Ala309Val
|
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NM_006516.4:c.926C>T
MANE Select
|
NP_006507.2:p.Ala309Val
|
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