ENST00000559133.6:c.5604A>T
|
ENSP00000453958.2:p.Thr1868=
|
|
ENST00000674301.2:c.5604A>T
|
ENSP00000501333.2:p.Thr1868=
|
|
ENST00000684448.1:n.4278A>T
|
|
|
ENST00000316623.10:c.5604A>T
MANE Select
|
ENSP00000325527.5:p.Thr1868=
|
|
ENST00000674301.1:c.603A>T
|
ENSP00000501333.1:p.Thr201=
|
|
ENST00000316623.9:c.5604A>T
|
ENSP00000325527.5:p.Thr1868=
|
|
ENST00000537463.6:c.*1367A>T
|
ENSP00000440294.2:n.*1367A>T
|
|
ENST00000559133.5:c.911A>T
|
|
|
NM_000138.4:c.5604A>T , LRG_778t1:c.5604A>T
|
NP_000129.3:p.Thr1868=
|
|
NM_000138.5:c.5604A>T
MANE Select
|
NP_000129.3:p.Thr1868=
|
|