ENST00000559133.6:c.6872A>C
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ENSP00000453958.2:p.Asp2291Ala
|
|
ENST00000674301.2:c.*323A>C
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ENSP00000501333.2:n.*323A>C
|
|
ENST00000682170.1:n.481A>C
|
|
|
ENST00000682767.1:n.107A>C
|
|
|
ENST00000316623.10:c.6872A>C
MANE Select
|
ENSP00000325527.5:p.Asp2291Ala
|
|
ENST00000674301.1:c.1976A>C
|
ENSP00000501333.1:n.1976A>C
|
|
ENST00000316623.9:c.6872A>C
|
ENSP00000325527.5:p.Asp2291Ala
|
|
ENST00000559133.5:c.2179A>C
|
|
|
ENST00000560720.1:n.159A>C
|
|
|
NM_000138.4:c.6872A>C , LRG_778t1:c.6872A>C
|
NP_000129.3:p.Asp2291Ala
|
|
NM_000138.5:c.6872A>C
MANE Select
|
NP_000129.3:p.Asp2291Ala
|
|