ENST00000559133.6:c.*1013A>G
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ENSP00000453958.2:n.*1013A>G
|
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ENST00000674301.2:c.*1718A>G
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ENSP00000501333.2:n.*1718A>G
|
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ENST00000682158.1:n.1586A>G
|
|
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ENST00000682170.1:n.2386A>G
|
|
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ENST00000682767.1:n.1502A>G
|
|
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ENST00000316623.10:c.8205A>G
MANE Select
|
ENSP00000325527.5:p.Glu2735=
|
|
ENST00000674301.1:c.3371A>G
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ENSP00000501333.1:n.3371A>G
|
|
ENST00000316623.9:c.8205A>G
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ENSP00000325527.5:p.Glu2735=
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ENST00000559133.5:c.3574A>G
|
|
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ENST00000561429.1:n.460A>G
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|
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NM_000138.4:c.8205A>G , LRG_778t1:c.8205A>G
|
NP_000129.3:p.Glu2735=
|
|
NM_000138.5:c.8205A>G
MANE Select
|
NP_000129.3:p.Glu2735=
|
|