ENST00000366930.9:c.*89A>G
MANE Select
|
ENSP00000355897.4:n.*89A>G
|
|
ENST00000366929.4:c.*89A>G
|
ENSP00000355896.4:n.*89A>G
|
|
ENST00000366930.8:c.*89A>G
|
ENSP00000355897.4:n.*89A>G
|
|
ENST00000479322.1:n.818A>G
|
|
|
NM_001135599.2:c.*89A>G
|
NP_001129071.1:n.*89A>G
|
|
NM_003238.3:c.*89A>G
|
NP_003229.1:n.*89A>G
|
|
NM_001135599.3:c.*89A>G
|
NP_001129071.1:n.*89A>G
|
|
NM_003238.4:c.*89A>G
|
NP_003229.1:n.*89A>G
|
|
NR_138148.1:n.2637A>G
|
|
|
NR_138149.1:n.2721A>G
|
|
|
NM_003238.5:c.*89A>G
|
NP_003229.1:n.*89A>G
|
|
NM_003238.6:c.*89A>G
MANE Select
|
NP_003229.1:n.*89A>G
|
|
NM_001135599.4:c.*89A>G
|
NP_001129071.1:n.*89A>G
|
|
NR_138148.2:n.2585A>G
|
|
|
NR_138149.2:n.2669A>G
|
|
|