ENST00000559133.6:c.6776C>A
|
ENSP00000453958.2:p.Thr2259Asn
|
|
ENST00000674301.2:c.*227C>A
|
ENSP00000501333.2:n.*227C>A
|
|
ENST00000682170.1:n.385C>A
|
|
|
ENST00000316623.10:c.6776C>A
MANE Select
|
ENSP00000325527.5:p.Thr2259Asn
|
|
ENST00000674301.1:c.1880C>A
|
ENSP00000501333.1:n.1880C>A
|
|
ENST00000316623.9:c.6776C>A
|
ENSP00000325527.5:p.Thr2259Asn
|
|
ENST00000537463.6:c.*2539C>A
|
ENSP00000440294.2:n.*2539C>A
|
|
ENST00000559133.5:c.2083C>A
|
|
|
ENST00000560720.1:n.63C>A
|
|
|
NM_000138.4:c.6776C>A , LRG_778t1:c.6776C>A
|
NP_000129.3:p.Thr2259Asn
|
|
NM_000138.5:c.6776C>A
MANE Select
|
NP_000129.3:p.Thr2259Asn
|
|