ENST00000578493.2:n.700T>C
|
|
|
ENST00000699291.1:c.492T>C
|
ENSP00000514272.1:p.Asp164=
|
|
ENST00000699292.1:n.407T>C
|
|
|
ENST00000225275.4:c.1367T>C
MANE Select
|
ENSP00000225275.3:p.Ile456Thr
|
|
ENST00000225275.3:c.1367T>C
|
ENSP00000225275.3:p.Ile456Thr
|
|
NM_000250.1:c.1367T>C , LRG_84t1:c.1367T>C
|
NP_000241.1:p.Ile456Thr
|
|
XM_011524821.1:c.1553T>C
|
XP_011523123.1:p.Ile518Thr
|
|
XM_011524822.1:c.1082T>C
|
XP_011523124.1:p.Ile361Thr
|
|
XM_011524823.1:c.1392T>C
|
XP_011523125.1:p.Asp464=
|
|
NM_000250.2:c.1367T>C
MANE Select
|
NP_000241.1:p.Ile456Thr
|
|