ENST00000376649.8:c.621G>T
MANE Select
|
ENSP00000365837.3:p.Thr207=
|
|
ENST00000322060.9:c.537G>T
|
ENSP00000324726.5:p.Thr179=
|
|
ENST00000376649.7:c.621G>T
|
ENSP00000365837.3:p.Thr207=
|
|
ENST00000443358.6:c.537G>T
|
ENSP00000392451.2:p.Thr179=
|
|
ENST00000535067.5:c.358-2171G>T
|
ENSP00000443969.1:n.358-2171G>T
|
|
ENST00000537484.1:c.546G>T
|
ENSP00000440179.1:p.Thr182=
|
|
ENST00000542167.2:c.462G>T
|
ENSP00000438948.1:p.Thr154=
|
|
ENST00000543754.1:n.442G>T
|
|
|
NM_001002019.2:c.537G>T
|
NP_001002019.1:p.Thr179=
|
|
NM_001002020.2:c.537G>T
|
NP_001002020.1:p.Thr179=
|
|
NM_025215.5:c.621G>T
|
NP_079491.2:p.Thr207=
|
|
XM_011538768.1:c.222G>T
|
XP_011537070.1:p.Thr74=
|
|
XM_011538768.3:c.222G>T
|
XP_011537070.1:p.Thr74=
|
|
XR_001748872.1:n.1076G>T
|
|
|
NM_001002019.3:c.537G>T
|
NP_001002019.1:p.Thr179=
|
|
NM_001002020.3:c.537G>T
|
NP_001002020.1:p.Thr179=
|
|
NM_025215.6:c.621G>T
MANE Select
|
NP_079491.2:p.Thr207=
|
|