ENST00000559133.6:c.6098A>C
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ENSP00000453958.2:p.Glu2033Ala
|
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ENST00000674301.2:c.6098A>C
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ENSP00000501333.2:p.Glu2033Ala
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ENST00000316623.10:c.6098A>C
MANE Select
|
ENSP00000325527.5:p.Glu2033Ala
|
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ENST00000674301.1:c.1097A>C
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ENSP00000501333.1:p.Glu366Ala
|
|
ENST00000316623.9:c.6098A>C
|
ENSP00000325527.5:p.Glu2033Ala
|
|
ENST00000537463.6:c.*1861A>C
|
ENSP00000440294.2:n.*1861A>C
|
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ENST00000559133.5:c.1405A>C
|
|
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ENST00000560820.1:n.218A>C
|
|
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NM_000138.4:c.6098A>C , LRG_778t1:c.6098A>C
|
NP_000129.3:p.Glu2033Ala
|
|
NM_000138.5:c.6098A>C
MANE Select
|
NP_000129.3:p.Glu2033Ala
|
|