ENST00000681999.1:n.1488A>T
|
|
|
ENST00000682451.1:n.1457A>T
|
|
|
ENST00000682975.1:n.1506A>T
|
|
|
ENST00000683894.1:c.1359A>T
|
ENSP00000507789.1:p.Thr453=
|
|
ENST00000684085.1:n.1488A>T
|
|
|
ENST00000684712.1:n.1719A>T
|
|
|
ENST00000403359.8:c.1611A>T
MANE Select
|
ENSP00000384823.4:p.Thr537=
|
|
ENST00000316377.8:c.1377A>T
|
ENSP00000323822.5:p.Thr459=
|
|
ENST00000402508.5:c.1359A>T
|
ENSP00000385398.1:p.Thr453=
|
|
ENST00000403359.7:c.1611A>T
|
ENSP00000384823.3:p.Thr537=
|
|
ENST00000492225.5:n.1459A>T
|
|
|
ENST00000493962.6:c.985A>T
|
|
|
NM_001190274.1:c.1611A>T
|
NP_001177203.1:p.Thr537=
|
|
NM_025133.4:c.1359A>T
|
NP_079409.3:p.Thr453=
|
|
XM_005264572.3:c.1611A>T
|
XP_005264629.1:p.Thr537=
|
|
XM_005264573.3:c.1608A>T
|
XP_005264630.1:p.Thr536=
|
|
XM_005264572.5:c.1611A>T
|
XP_005264629.1:p.Thr537=
|
|
XM_005264573.5:c.1608A>T
|
XP_005264630.1:p.Thr536=
|
|
XM_017005015.1:c.1608A>T
|
XP_016860504.1:p.Thr536=
|
|
XM_017005016.2:c.1359A>T
|
XP_016860505.1:p.Thr453=
|
|
XM_017005017.1:c.1359A>T
|
XP_016860506.1:p.Thr453=
|
|
NM_001190274.2:c.1611A>T
MANE Select
|
NP_001177203.1:p.Thr537=
|
|
NM_001374325.1:c.1359A>T
|
NP_001361254.1:p.Thr453=
|
|