ENST00000216124.10:c.*922G=
MANE Select
|
ENSP00000216124.5:n.*922G=
|
|
ENST00000608497.1:c.181-328G=
|
|
|
NM_000487.5:c.*922G=
|
NP_000478.3:n.*922G=
|
|
NM_001085425.2:c.*922G=
|
NP_001078894.2:n.*922G=
|
|
NM_001085426.2:c.*922G=
|
NP_001078895.2:n.*922G=
|
|
NM_001085427.2:c.*922G=
|
NP_001078896.2:n.*922G=
|
|
NM_001085428.2:c.*922G=
|
NP_001078897.1:n.*922G=
|
|
NM_001362782.1:c.*922G=
|
NP_001349711.1:n.*922G=
|
|
NM_000487.6:c.*922G=
MANE Select
|
NP_000478.3:n.*922G=
|
|
NM_001085425.3:c.*922G=
|
NP_001078894.2:n.*922G=
|
|
NM_001085426.3:c.*922G=
|
NP_001078895.2:n.*922G=
|
|
NM_001085427.3:c.*922G=
|
NP_001078896.2:n.*922G=
|
|
NM_001085428.3:c.*922G=
|
NP_001078897.1:n.*922G=
|
|
NM_001362782.2:c.*922G=
|
NP_001349711.1:n.*922G=
|
|