ENST00000559133.6:c.*1277G>C
|
ENSP00000453958.2:n.*1277G>C
|
|
ENST00000674301.2:c.*1982G>C
|
ENSP00000501333.2:n.*1982G>C
|
|
ENST00000682158.1:n.1850G>C
|
|
|
ENST00000682170.1:n.2650G>C
|
|
|
ENST00000682767.1:n.1766G>C
|
|
|
ENST00000316623.10:c.8469G>C
MANE Select
|
ENSP00000325527.5:p.Val2823=
|
|
ENST00000674301.1:c.3635G>C
|
ENSP00000501333.1:n.3635G>C
|
|
ENST00000316623.9:c.8469G>C
|
ENSP00000325527.5:p.Val2823=
|
|
ENST00000559133.5:c.3838G>C
|
|
|
NM_000138.4:c.8469G>C , LRG_778t1:c.8469G>C
|
NP_000129.3:p.Val2823=
|
|
NM_000138.5:c.8469G>C
MANE Select
|
NP_000129.3:p.Val2823=
|
|