ENST00000578493.2:n.1021T>C
|
|
|
ENST00000699291.1:c.813T>C
|
ENSP00000514272.1:n.813T>C
|
|
ENST00000699292.1:n.1223T>C
|
|
|
ENST00000225275.4:c.1688T>C
MANE Select
|
ENSP00000225275.3:p.Ile563Thr
|
|
ENST00000225275.3:c.1688T>C
|
ENSP00000225275.3:p.Ile563Thr
|
|
ENST00000577220.1:c.146T>C
|
ENSP00000464668.1:p.Ile49Thr
|
|
NM_000250.1:c.1688T>C , LRG_84t1:c.1688T>C
|
NP_000241.1:p.Ile563Thr
|
|
XM_011524821.1:c.1874T>C
|
XP_011523123.1:p.Ile625Thr
|
|
XM_011524822.1:c.1403T>C
|
XP_011523124.1:p.Ile468Thr
|
|
NM_000250.2:c.1688T>C
MANE Select
|
NP_000241.1:p.Ile563Thr
|
|