ENST00000559133.6:c.*1265G>A
|
ENSP00000453958.2:n.*1265G>A
|
|
ENST00000674301.2:c.*1970G>A
|
ENSP00000501333.2:n.*1970G>A
|
|
ENST00000682158.1:n.1838G>A
|
|
|
ENST00000682170.1:n.2638G>A
|
|
|
ENST00000682767.1:n.1754G>A
|
|
|
ENST00000316623.10:c.8457G>A
MANE Select
|
ENSP00000325527.5:p.Lys2819=
|
|
ENST00000674301.1:c.3623G>A
|
ENSP00000501333.1:n.3623G>A
|
|
ENST00000316623.9:c.8457G>A
|
ENSP00000325527.5:p.Lys2819=
|
|
ENST00000559133.5:c.3826G>A
|
|
|
NM_000138.4:c.8457G>A , LRG_778t1:c.8457G>A
|
NP_000129.3:p.Lys2819=
|
|
NM_000138.5:c.8457G>A
MANE Select
|
NP_000129.3:p.Lys2819=
|
|