ENST00000355943.8:c.*102G>T
MANE Select
|
ENSP00000348211.3:n.*102G>T
|
|
ENST00000355943.7:c.*102G>T
|
ENSP00000348211.3:n.*102G>T
|
|
ENST00000447245.6:c.*102G>T
|
ENSP00000399717.2:n.*102G>T
|
|
ENST00000504098.1:c.*102G>T
|
ENSP00000425708.1:n.*102G>T
|
|
ENST00000509432.1:c.*102G>T
|
ENSP00000426604.1:n.*102G>T
|
|
ENST00000513706.2:n.2959G>T
|
|
|
ENST00000513807.5:c.*102G>T
|
ENSP00000421134.1:n.*102G>T
|
|
NM_001303249.1:c.*102G>T
|
NP_001290178.1:n.*102G>T
|
|
NM_001303250.1:c.*102G>T
|
NP_001290179.1:n.*102G>T
|
|
NM_138773.2:c.*102G>T
|
NP_620128.1:n.*102G>T
|
|
NM_001303249.2:c.*102G>T
|
NP_001290178.1:n.*102G>T
|
|
NM_001303250.2:c.*102G>T
|
NP_001290179.1:n.*102G>T
|
|
NM_138773.3:c.*102G>T
|
NP_620128.1:n.*102G>T
|
|
NR_138151.1:n.1633G>T
|
|
|
NM_138773.4:c.*102G>T
MANE Select
|
NP_620128.1:n.*102G>T
|
|
NM_001303249.3:c.*102G>T
|
NP_001290178.1:n.*102G>T
|
|
NM_001303250.3:c.*102G>T
|
NP_001290179.1:n.*102G>T
|
|
NR_138151.2:n.1598G>T
|
|
|