ENST00000559133.6:c.6779A>C
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ENSP00000453958.2:p.Glu2260Ala
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ENST00000674301.2:c.*230A>C
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ENSP00000501333.2:n.*230A>C
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ENST00000682170.1:n.388A>C
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|
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ENST00000316623.10:c.6779A>C
MANE Select
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ENSP00000325527.5:p.Glu2260Ala
|
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ENST00000674301.1:c.1883A>C
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ENSP00000501333.1:n.1883A>C
|
|
ENST00000316623.9:c.6779A>C
|
ENSP00000325527.5:p.Glu2260Ala
|
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ENST00000559133.5:c.2086A>C
|
|
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ENST00000560720.1:n.66A>C
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|
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NM_000138.4:c.6779A>C , LRG_778t1:c.6779A>C
|
NP_000129.3:p.Glu2260Ala
|
|
NM_000138.5:c.6779A>C
MANE Select
|
NP_000129.3:p.Glu2260Ala
|
|