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NM_001080.3:c.651C>T
MANE Select
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NP_001071.1:p.Ala217=
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ENST00000357578.8:c.651C>T
MANE Select
|
ENSP00000350191.3:p.Ala217=
|
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NM_001368954.1:c.651C>T
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NP_001355883.1:p.Ala217=
|
|
NM_170740.1:c.651C>T
|
NP_733936.1:p.Ala217=
|
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ENST00000348925.2:c.651C>T
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ENSP00000314649.3:p.Ala217=
|
|
ENST00000357578.7:c.651C>T
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ENSP00000350191.3:p.Ala217=
|
|
ENST00000491546.5:c.567C>T
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ENSP00000417687.1:p.Ala189=
|
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ENST00000672352.1:c.414C>T
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ENSP00000500876.1:p.Ala138=
|
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ENST00000672557.1:c.569C>T
|
|
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ENST00000672619.1:n.11C>T
|
|
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ENST00000672652.1:c.572C>T
|
|
|
ENST00000675422.1:n.1411C>T
|
|