ENST00000527168.6:n.921A>T
|
|
|
ENST00000529110.2:c.906A>T
|
ENSP00000435349.2:p.Thr302=
|
|
ENST00000529957.6:n.880A>T
|
|
|
ENST00000683366.1:c.*554A>T
|
ENSP00000507283.1:n.*554A>T
|
|
ENST00000683887.1:c.870A>T
|
ENSP00000506886.1:p.Thr290=
|
|
ENST00000684100.1:n.816A>T
|
|
|
ENST00000684126.1:n.956A>T
|
|
|
ENST00000684688.1:n.1447A>T
|
|
|
ENST00000204679.9:c.822A>T
MANE Select
|
ENSP00000204679.4:p.Thr274=
|
|
ENST00000204679.8:c.822A>T
|
ENSP00000204679.4:p.Thr274=
|
|
ENST00000527076.1:n.2045A>T
|
|
|
ENST00000527168.5:n.989A>T
|
|
|
ENST00000529957.5:n.921A>T
|
|
|
NM_032520.4:c.822A>T
|
NP_115909.1:p.Thr274=
|
|
XM_017023782.1:c.870A>T
|
XP_016879271.1:p.Thr290=
|
|
XM_017023783.1:c.462A>T
|
XP_016879272.1:p.Thr154=
|
|
NM_032520.5:c.822A>T
MANE Select
|
NP_115909.1:p.Thr274=
|
|