ENST00000253122.10:c.1052C>T
MANE Select
|
ENSP00000253122.5:p.Thr351Ile
|
|
ENST00000253122.9:c.1052C>T
|
ENSP00000253122.5:p.Thr351Ile
|
|
ENST00000413787.1:c.168C>T
|
ENSP00000400463.1:p.Asp56=
|
|
ENST00000430077.6:c.707C>T
|
ENSP00000403041.2:p.Thr236Ile
|
|
ENST00000442457.1:c.106C>T
|
|
|
ENST00000457723.1:c.36C>T
|
ENSP00000394742.1:p.Asp12=
|
|
ENST00000467402.1:n.151C>T
|
|
|
ENST00000485324.1:n.1085C>T
|
|
|
NM_001142805.1:c.1022C>T
|
NP_001136277.1:p.Thr341Ile
|
|
NM_001142806.1:c.707C>T
|
NP_001136278.1:p.Thr236Ile
|
|
NM_005629.3:c.1052C>T
|
NP_005620.1:p.Thr351Ile
|
|
NM_005629.4:c.1052C>T
MANE Select
|
NP_005620.1:p.Thr351Ile
|
|
NM_001142805.2:c.1022C>T
|
NP_001136277.1:p.Thr341Ile
|
|