ENST00000355943.8:c.1226T>C
MANE Select
|
ENSP00000348211.3:p.Ile409Thr
|
|
ENST00000355943.7:c.1226T>C
|
ENSP00000348211.3:p.Ile409Thr
|
|
ENST00000447245.6:c.983T>C
|
ENSP00000399717.2:p.Ile328Thr
|
|
ENST00000504098.1:c.788T>C
|
ENSP00000425708.1:p.Ile263Thr
|
|
ENST00000509432.1:c.587T>C
|
ENSP00000426604.1:p.Ile196Thr
|
|
ENST00000513706.2:n.2826T>C
|
|
|
ENST00000513807.5:c.740T>C
|
ENSP00000421134.1:p.Ile247Thr
|
|
NM_001303249.1:c.983T>C
|
NP_001290178.1:p.Ile328Thr
|
|
NM_001303250.1:c.953T>C
|
NP_001290179.1:p.Ile318Thr
|
|
NM_138773.2:c.1226T>C
|
NP_620128.1:p.Ile409Thr
|
|
NM_001303249.2:c.983T>C
|
NP_001290178.1:p.Ile328Thr
|
|
NM_001303250.2:c.953T>C
|
NP_001290179.1:p.Ile318Thr
|
|
NM_138773.3:c.1226T>C
|
NP_620128.1:p.Ile409Thr
|
|
NR_138151.1:n.1500T>C
|
|
|
NM_138773.4:c.1226T>C
MANE Select
|
NP_620128.1:p.Ile409Thr
|
|
NM_001303249.3:c.983T>C
|
NP_001290178.1:p.Ile328Thr
|
|
NM_001303250.3:c.953T>C
|
NP_001290179.1:p.Ile318Thr
|
|
NR_138151.2:n.1465T>C
|
|
|