ENST00000559133.6:c.6066A>G
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ENSP00000453958.2:p.Glu2022=
|
|
ENST00000674301.2:c.6066A>G
|
ENSP00000501333.2:p.Glu2022=
|
|
ENST00000316623.10:c.6066A>G
MANE Select
|
ENSP00000325527.5:p.Glu2022=
|
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ENST00000674301.1:c.1065A>G
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ENSP00000501333.1:p.Glu355=
|
|
ENST00000316623.9:c.6066A>G
|
ENSP00000325527.5:p.Glu2022=
|
|
ENST00000537463.6:c.*1829A>G
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ENSP00000440294.2:n.*1829A>G
|
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ENST00000559133.5:c.1373A>G
|
|
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ENST00000560820.1:n.186A>G
|
|
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NM_000138.4:c.6066A>G , LRG_778t1:c.6066A>G
|
NP_000129.3:p.Glu2022=
|
|
NM_000138.5:c.6066A>G
MANE Select
|
NP_000129.3:p.Glu2022=
|
|