ENST00000559133.6:c.6609A>C
|
ENSP00000453958.2:p.Thr2203=
|
|
ENST00000674301.2:c.6609A>C
|
ENSP00000501333.2:p.Thr2203=
|
|
ENST00000682170.1:n.218A>C
|
|
|
ENST00000316623.10:c.6609A>C
MANE Select
|
ENSP00000325527.5:p.Thr2203=
|
|
ENST00000674301.1:c.1608A>C
|
ENSP00000501333.1:p.Thr536=
|
|
ENST00000316623.9:c.6609A>C
|
ENSP00000325527.5:p.Thr2203=
|
|
ENST00000537463.6:c.*2372A>C
|
ENSP00000440294.2:n.*2372A>C
|
|
ENST00000559133.5:c.1916A>C
|
|
|
NM_000138.4:c.6609A>C , LRG_778t1:c.6609A>C
|
NP_000129.3:p.Thr2203=
|
|
NM_000138.5:c.6609A>C
MANE Select
|
NP_000129.3:p.Thr2203=
|
|