ENST00000355943.8:c.1043C>T
MANE Select
|
ENSP00000348211.3:p.Thr348Ile
|
|
ENST00000355943.7:c.1043C>T
|
ENSP00000348211.3:p.Thr348Ile
|
|
ENST00000447245.6:c.800C>T
|
ENSP00000399717.2:p.Thr267Ile
|
|
ENST00000502462.6:n.1359C>T
|
|
|
ENST00000504098.1:c.605C>T
|
ENSP00000425708.1:p.Thr202Ile
|
|
ENST00000509432.1:c.404C>T
|
ENSP00000426604.1:p.Thr135Ile
|
|
ENST00000513706.2:n.2643C>T
|
|
|
ENST00000513807.5:c.557C>T
|
ENSP00000421134.1:p.Thr186Ile
|
|
NM_001303249.1:c.800C>T
|
NP_001290178.1:p.Thr267Ile
|
|
NM_001303250.1:c.770C>T
|
NP_001290179.1:p.Thr257Ile
|
|
NM_138773.2:c.1043C>T
|
NP_620128.1:p.Thr348Ile
|
|
NM_001303249.2:c.800C>T
|
NP_001290178.1:p.Thr267Ile
|
|
NM_001303250.2:c.770C>T
|
NP_001290179.1:p.Thr257Ile
|
|
NM_138773.3:c.1043C>T
|
NP_620128.1:p.Thr348Ile
|
|
NR_138151.1:n.1317C>T
|
|
|
NM_138773.4:c.1043C>T
MANE Select
|
NP_620128.1:p.Thr348Ile
|
|
NM_001303249.3:c.800C>T
|
NP_001290178.1:p.Thr267Ile
|
|
NM_001303250.3:c.770C>T
|
NP_001290179.1:p.Thr257Ile
|
|
NR_138151.2:n.1282C>T
|
|
|