ENST00000366669.9:c.1819T>G
MANE Select
|
ENSP00000355629.4:p.Tyr607Asp
|
|
ENST00000366668.7:c.1816T>G
|
ENSP00000355628.3:p.Tyr606Asp
|
|
ENST00000366669.8:c.1819T>G
|
ENSP00000355629.4:p.Tyr607Asp
|
|
ENST00000468893.6:c.*1677T>G
|
ENSP00000476305.1:n.*1677T>G
|
|
ENST00000478710.1:n.78T>G
|
|
|
ENST00000490900.1:n.598T>G
|
|
|
ENST00000534989.1:c.1642T>G
|
ENSP00000440349.1:p.Tyr548Asp
|
|
NM_001145036.1:c.1816T>G
|
NP_001138508.1:p.Tyr606Asp
|
|
NM_007357.2:c.1819T>G
|
NP_031383.1:p.Tyr607Asp
|
|
NM_007357.3:c.1819T>G
MANE Select
|
NP_031383.1:p.Tyr607Asp
|
|
NM_001145036.2:c.1816T>G
|
NP_001138508.1:p.Tyr606Asp
|
|