ENST00000380649.8:c.1129G>T
MANE Select
|
ENSP00000370023.3:p.Ala377Ser
|
|
ENST00000492433.2:c.1129G>T
|
ENSP00000438039.2:p.Ala377Ser
|
|
ENST00000643057.1:c.*1020G>T
|
ENSP00000493761.1:n.*1020G>T
|
|
ENST00000643063.1:c.*175G>T
|
ENSP00000495353.1:n.*175G>T
|
|
ENST00000643233.1:c.*1020G>T
|
ENSP00000493880.1:n.*1020G>T
|
|
ENST00000644428.1:c.1129G>T
|
ENSP00000495560.1:p.Ala377Ser
|
|
ENST00000645274.1:c.1024G>T
|
ENSP00000493996.1:p.Ala342Ser
|
|
ENST00000646031.1:c.488G>T
|
|
|
ENST00000646483.1:c.995G>T
|
ENSP00000496185.1:n.995G>T
|
|
ENST00000380649.7:c.1129G>T
|
ENSP00000370023.3:p.Ala377Ser
|
|
NM_000182.4:c.1129G>T
|
NP_000173.2:p.Ala377Ser
|
|
NM_000182.5:c.1129G>T
MANE Select
|
NP_000173.2:p.Ala377Ser
|
|