ENST00000559133.6:c.*1256C>G
|
ENSP00000453958.2:n.*1256C>G
|
|
ENST00000674301.2:c.*1961C>G
|
ENSP00000501333.2:n.*1961C>G
|
|
ENST00000682158.1:n.1829C>G
|
|
|
ENST00000682170.1:n.2629C>G
|
|
|
ENST00000682767.1:n.1745C>G
|
|
|
ENST00000316623.10:c.8448C>G
MANE Select
|
ENSP00000325527.5:p.His2816Gln
|
|
ENST00000674301.1:c.3614C>G
|
ENSP00000501333.1:n.3614C>G
|
|
ENST00000316623.9:c.8448C>G
|
ENSP00000325527.5:p.His2816Gln
|
|
ENST00000559133.5:c.3817C>G
|
|
|
NM_000138.4:c.8448C>G , LRG_778t1:c.8448C>G
|
NP_000129.3:p.His2816Gln
|
|
NM_000138.5:c.8448C>G
MANE Select
|
NP_000129.3:p.His2816Gln
|
|