ENST00000559133.6:c.*1309C>A
|
ENSP00000453958.2:n.*1309C>A
|
|
ENST00000674301.2:c.*2014C>A
|
ENSP00000501333.2:n.*2014C>A
|
|
ENST00000682158.1:n.1882C>A
|
|
|
ENST00000682170.1:n.2682C>A
|
|
|
ENST00000682767.1:n.1798C>A
|
|
|
ENST00000316623.10:c.8501C>A
MANE Select
|
ENSP00000325527.5:p.Thr2834Asn
|
|
ENST00000674301.1:c.3667C>A
|
ENSP00000501333.1:n.3667C>A
|
|
ENST00000316623.9:c.8501C>A
|
ENSP00000325527.5:p.Thr2834Asn
|
|
ENST00000559133.5:c.3870C>A
|
|
|
NM_000138.4:c.8501C>A , LRG_778t1:c.8501C>A
|
NP_000129.3:p.Thr2834Asn
|
|
NM_000138.5:c.8501C>A
MANE Select
|
NP_000129.3:p.Thr2834Asn
|
|