ENST00000559133.6:c.*754T>A
|
ENSP00000453958.2:n.*754T>A
|
|
ENST00000674301.2:c.*1459T>A
|
ENSP00000501333.2:n.*1459T>A
|
|
ENST00000682158.1:n.1327T>A
|
|
|
ENST00000682170.1:n.2127T>A
|
|
|
ENST00000682767.1:n.1243T>A
|
|
|
ENST00000316623.10:c.7946T>A
MANE Select
|
ENSP00000325527.5:p.Ile2649Asn
|
|
ENST00000674301.1:c.3112T>A
|
ENSP00000501333.1:n.3112T>A
|
|
ENST00000316623.9:c.7946T>A
|
ENSP00000325527.5:p.Ile2649Asn
|
|
ENST00000559133.5:c.3315T>A
|
|
|
ENST00000561429.1:n.201T>A
|
|
|
NM_000138.4:c.7946T>A , LRG_778t1:c.7946T>A
|
NP_000129.3:p.Ile2649Asn
|
|
NM_000138.5:c.7946T>A
MANE Select
|
NP_000129.3:p.Ile2649Asn
|
|