ENST00000559133.6:c.6908A>T
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ENSP00000453958.2:p.Glu2303Val
|
|
ENST00000674301.2:c.*359A>T
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ENSP00000501333.2:n.*359A>T
|
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ENST00000682170.1:n.517A>T
|
|
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ENST00000682767.1:n.143A>T
|
|
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ENST00000316623.10:c.6908A>T
MANE Select
|
ENSP00000325527.5:p.Glu2303Val
|
|
ENST00000674301.1:c.2012A>T
|
ENSP00000501333.1:n.2012A>T
|
|
ENST00000316623.9:c.6908A>T
|
ENSP00000325527.5:p.Glu2303Val
|
|
ENST00000559133.5:c.2215A>T
|
|
|
ENST00000560720.1:n.195A>T
|
|
|
NM_000138.4:c.6908A>T , LRG_778t1:c.6908A>T
|
NP_000129.3:p.Glu2303Val
|
|
NM_000138.5:c.6908A>T
MANE Select
|
NP_000129.3:p.Glu2303Val
|
|