ENST00000366930.9:c.*181C>T
MANE Select
|
ENSP00000355897.4:n.*181C>T
|
|
ENST00000366929.4:c.*181C>T
|
ENSP00000355896.4:n.*181C>T
|
|
ENST00000366930.8:c.*181C>T
|
ENSP00000355897.4:n.*181C>T
|
|
ENST00000479322.1:n.910C>T
|
|
|
NM_001135599.2:c.*181C>T
|
NP_001129071.1:n.*181C>T
|
|
NM_003238.3:c.*181C>T
|
NP_003229.1:n.*181C>T
|
|
NM_001135599.3:c.*181C>T
|
NP_001129071.1:n.*181C>T
|
|
NM_003238.4:c.*181C>T
|
NP_003229.1:n.*181C>T
|
|
NR_138148.1:n.2729C>T
|
|
|
NR_138149.1:n.2813C>T
|
|
|
NM_003238.5:c.*181C>T
|
NP_003229.1:n.*181C>T
|
|
NM_003238.6:c.*181C>T
MANE Select
|
NP_003229.1:n.*181C>T
|
|
NM_001135599.4:c.*181C>T
|
NP_001129071.1:n.*181C>T
|
|
NR_138148.2:n.2677C>T
|
|
|
NR_138149.2:n.2761C>T
|
|
|