ENST00000559133.6:c.*1111T>C
|
ENSP00000453958.2:n.*1111T>C
|
|
ENST00000674301.2:c.*1816T>C
|
ENSP00000501333.2:n.*1816T>C
|
|
ENST00000682158.1:n.1684T>C
|
|
|
ENST00000682170.1:n.2484T>C
|
|
|
ENST00000682767.1:n.1600T>C
|
|
|
ENST00000316623.10:c.8303T>C
MANE Select
|
ENSP00000325527.5:p.Ile2768Thr
|
|
ENST00000674301.1:c.3469T>C
|
ENSP00000501333.1:n.3469T>C
|
|
ENST00000316623.9:c.8303T>C
|
ENSP00000325527.5:p.Ile2768Thr
|
|
ENST00000559133.5:c.3672T>C
|
|
|
ENST00000561429.1:n.558T>C
|
|
|
NM_000138.4:c.8303T>C , LRG_778t1:c.8303T>C
|
NP_000129.3:p.Ile2768Thr
|
|
NM_000138.5:c.8303T>C
MANE Select
|
NP_000129.3:p.Ile2768Thr
|
|