ENST00000559133.6:c.*1084A>G
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ENSP00000453958.2:n.*1084A>G
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ENST00000674301.2:c.*1789A>G
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ENSP00000501333.2:n.*1789A>G
|
|
ENST00000682158.1:n.1657A>G
|
|
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ENST00000682170.1:n.2457A>G
|
|
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ENST00000682767.1:n.1573A>G
|
|
|
ENST00000316623.10:c.8276A>G
MANE Select
|
ENSP00000325527.5:p.Glu2759Gly
|
|
ENST00000674301.1:c.3442A>G
|
ENSP00000501333.1:n.3442A>G
|
|
ENST00000316623.9:c.8276A>G
|
ENSP00000325527.5:p.Glu2759Gly
|
|
ENST00000559133.5:c.3645A>G
|
|
|
ENST00000561429.1:n.531A>G
|
|
|
NM_000138.4:c.8276A>G , LRG_778t1:c.8276A>G
|
NP_000129.3:p.Glu2759Gly
|
|
NM_000138.5:c.8276A>G
MANE Select
|
NP_000129.3:p.Glu2759Gly
|
|