ENST00000366930.9:c.*155G>T
MANE Select
|
ENSP00000355897.4:n.*155G>T
|
|
ENST00000366929.4:c.*155G>T
|
ENSP00000355896.4:n.*155G>T
|
|
ENST00000366930.8:c.*155G>T
|
ENSP00000355897.4:n.*155G>T
|
|
ENST00000479322.1:n.884G>T
|
|
|
NM_001135599.2:c.*155G>T
|
NP_001129071.1:n.*155G>T
|
|
NM_003238.3:c.*155G>T
|
NP_003229.1:n.*155G>T
|
|
NM_001135599.3:c.*155G>T
|
NP_001129071.1:n.*155G>T
|
|
NM_003238.4:c.*155G>T
|
NP_003229.1:n.*155G>T
|
|
NR_138148.1:n.2703G>T
|
|
|
NR_138149.1:n.2787G>T
|
|
|
NM_003238.5:c.*155G>T
|
NP_003229.1:n.*155G>T
|
|
NM_003238.6:c.*155G>T
MANE Select
|
NP_003229.1:n.*155G>T
|
|
NM_001135599.4:c.*155G>T
|
NP_001129071.1:n.*155G>T
|
|
NR_138148.2:n.2651G>T
|
|
|
NR_138149.2:n.2735G>T
|
|
|