ENST00000559133.6:c.*692C>T
|
ENSP00000453958.2:n.*692C>T
|
|
ENST00000674301.2:c.*1397C>T
|
ENSP00000501333.2:n.*1397C>T
|
|
ENST00000682158.1:n.1265C>T
|
|
|
ENST00000682170.1:n.2065C>T
|
|
|
ENST00000682767.1:n.1181C>T
|
|
|
ENST00000316623.10:c.7884C>T
MANE Select
|
ENSP00000325527.5:p.Ser2628=
|
|
ENST00000674301.1:c.3050C>T
|
ENSP00000501333.1:n.3050C>T
|
|
ENST00000316623.9:c.7884C>T
|
ENSP00000325527.5:p.Ser2628=
|
|
ENST00000559133.5:c.3253C>T
|
|
|
ENST00000561429.1:n.139C>T
|
|
|
NM_000138.4:c.7884C>T , LRG_778t1:c.7884C>T
|
NP_000129.3:p.Ser2628=
|
|
NM_000138.5:c.7884C>T
MANE Select
|
NP_000129.3:p.Ser2628=
|
|