ENST00000559133.6:c.*1030T=
|
ENSP00000453958.2:n.*1030T=
|
|
ENST00000674301.2:c.*1735T=
|
ENSP00000501333.2:n.*1735T=
|
|
ENST00000682158.1:n.1603T=
|
|
|
ENST00000682170.1:n.2403T=
|
|
|
ENST00000682767.1:n.1519T=
|
|
|
ENST00000316623.10:c.8222T=
MANE Select
|
ENSP00000325527.5:p.Ile2741=
|
|
ENST00000674301.1:c.3388T=
|
ENSP00000501333.1:n.3388T=
|
|
ENST00000316623.9:c.8222T=
|
ENSP00000325527.5:p.Ile2741=
|
|
ENST00000559133.5:c.3591T=
|
|
|
ENST00000561429.1:n.477T=
|
|
|
NM_000138.4:c.8222T= , LRG_778t1:c.8222T=
|
NP_000129.3:p.Ile2741=
|
|
NM_000138.5:c.8222T=
MANE Select
|
NP_000129.3:p.Ile2741=
|
|