ENST00000380649.8:c.1127T>G
MANE Select
|
ENSP00000370023.3:p.Ile376Ser
|
|
ENST00000492433.2:c.1127T>G
|
ENSP00000438039.2:p.Ile376Ser
|
|
ENST00000643057.1:c.*1018T>G
|
ENSP00000493761.1:n.*1018T>G
|
|
ENST00000643063.1:c.*173T>G
|
ENSP00000495353.1:n.*173T>G
|
|
ENST00000643233.1:c.*1018T>G
|
ENSP00000493880.1:n.*1018T>G
|
|
ENST00000644428.1:c.1127T>G
|
ENSP00000495560.1:p.Ile376Ser
|
|
ENST00000645274.1:c.1022T>G
|
ENSP00000493996.1:p.Ile341Ser
|
|
ENST00000646031.1:c.486T>G
|
|
|
ENST00000646483.1:c.993T>G
|
ENSP00000496185.1:n.993T>G
|
|
ENST00000380649.7:c.1127T>G
|
ENSP00000370023.3:p.Ile376Ser
|
|
NM_000182.4:c.1127T>G
|
NP_000173.2:p.Ile376Ser
|
|
NM_000182.5:c.1127T>G
MANE Select
|
NP_000173.2:p.Ile376Ser
|
|