ENST00000380649.8:c.1163T>C
MANE Select
|
ENSP00000370023.3:p.Ile388Thr
|
|
ENST00000492433.2:c.1163T>C
|
ENSP00000438039.2:p.Ile388Thr
|
|
ENST00000643057.1:c.*1054T>C
|
ENSP00000493761.1:n.*1054T>C
|
|
ENST00000643063.1:c.*209T>C
|
ENSP00000495353.1:n.*209T>C
|
|
ENST00000643233.1:c.*1054T>C
|
ENSP00000493880.1:n.*1054T>C
|
|
ENST00000644428.1:c.1163T>C
|
ENSP00000495560.1:p.Ile388Thr
|
|
ENST00000645274.1:c.1058T>C
|
ENSP00000493996.1:p.Ile353Thr
|
|
ENST00000646031.1:c.522T>C
|
|
|
ENST00000646483.1:c.1029T>C
|
ENSP00000496185.1:n.1029T>C
|
|
ENST00000380649.7:c.1163T>C
|
ENSP00000370023.3:p.Ile388Thr
|
|
NM_000182.4:c.1163T>C
|
NP_000173.2:p.Ile388Thr
|
|
NM_000182.5:c.1163T>C
MANE Select
|
NP_000173.2:p.Ile388Thr
|
|