ENST00000559133.6:c.*1292A>C
|
ENSP00000453958.2:n.*1292A>C
|
|
ENST00000674301.2:c.*1997A>C
|
ENSP00000501333.2:n.*1997A>C
|
|
ENST00000682158.1:n.1865A>C
|
|
|
ENST00000682170.1:n.2665A>C
|
|
|
ENST00000682767.1:n.1781A>C
|
|
|
ENST00000316623.10:c.8484A>C
MANE Select
|
ENSP00000325527.5:p.Ser2828=
|
|
ENST00000674301.1:c.3650A>C
|
ENSP00000501333.1:n.3650A>C
|
|
ENST00000316623.9:c.8484A>C
|
ENSP00000325527.5:p.Ser2828=
|
|
ENST00000559133.5:c.3853A>C
|
|
|
NM_000138.4:c.8484A>C , LRG_778t1:c.8484A>C
|
NP_000129.3:p.Ser2828=
|
|
NM_000138.5:c.8484A>C
MANE Select
|
NP_000129.3:p.Ser2828=
|
|