ENST00000366930.9:c.*162T>G
MANE Select
|
ENSP00000355897.4:n.*162T>G
|
|
ENST00000366929.4:c.*162T>G
|
ENSP00000355896.4:n.*162T>G
|
|
ENST00000366930.8:c.*162T>G
|
ENSP00000355897.4:n.*162T>G
|
|
ENST00000479322.1:n.891T>G
|
|
|
NM_001135599.2:c.*162T>G
|
NP_001129071.1:n.*162T>G
|
|
NM_003238.3:c.*162T>G
|
NP_003229.1:n.*162T>G
|
|
NM_001135599.3:c.*162T>G
|
NP_001129071.1:n.*162T>G
|
|
NM_003238.4:c.*162T>G
|
NP_003229.1:n.*162T>G
|
|
NR_138148.1:n.2710T>G
|
|
|
NR_138149.1:n.2794T>G
|
|
|
NM_003238.5:c.*162T>G
|
NP_003229.1:n.*162T>G
|
|
NM_003238.6:c.*162T>G
MANE Select
|
NP_003229.1:n.*162T>G
|
|
NM_001135599.4:c.*162T>G
|
NP_001129071.1:n.*162T>G
|
|
NR_138148.2:n.2658T>G
|
|
|
NR_138149.2:n.2742T>G
|
|
|