ENST00000559133.6:c.*1063G=
|
ENSP00000453958.2:n.*1063G=
|
|
ENST00000674301.2:c.*1768G=
|
ENSP00000501333.2:n.*1768G=
|
|
ENST00000682158.1:n.1636G=
|
|
|
ENST00000682170.1:n.2436G=
|
|
|
ENST00000682767.1:n.1552G=
|
|
|
ENST00000316623.10:c.8255G=
MANE Select
|
ENSP00000325527.5:p.Ser2752=
|
|
ENST00000674301.1:c.3421G=
|
ENSP00000501333.1:n.3421G=
|
|
ENST00000316623.9:c.8255G=
|
ENSP00000325527.5:p.Ser2752=
|
|
ENST00000559133.5:c.3624G=
|
|
|
ENST00000561429.1:n.510G=
|
|
|
NM_000138.4:c.8255G= , LRG_778t1:c.8255G=
|
NP_000129.3:p.Ser2752=
|
|
NM_000138.5:c.8255G=
MANE Select
|
NP_000129.3:p.Ser2752=
|
|