ENST00000366930.9:c.*174G>A
MANE Select
|
ENSP00000355897.4:n.*174G>A
|
|
ENST00000366929.4:c.*174G>A
|
ENSP00000355896.4:n.*174G>A
|
|
ENST00000366930.8:c.*174G>A
|
ENSP00000355897.4:n.*174G>A
|
|
ENST00000479322.1:n.903G>A
|
|
|
NM_001135599.2:c.*174G>A
|
NP_001129071.1:n.*174G>A
|
|
NM_003238.3:c.*174G>A
|
NP_003229.1:n.*174G>A
|
|
NM_001135599.3:c.*174G>A
|
NP_001129071.1:n.*174G>A
|
|
NM_003238.4:c.*174G>A
|
NP_003229.1:n.*174G>A
|
|
NR_138148.1:n.2722G>A
|
|
|
NR_138149.1:n.2806G>A
|
|
|
NM_003238.5:c.*174G>A
|
NP_003229.1:n.*174G>A
|
|
NM_003238.6:c.*174G>A
MANE Select
|
NP_003229.1:n.*174G>A
|
|
NM_001135599.4:c.*174G>A
|
NP_001129071.1:n.*174G>A
|
|
NR_138148.2:n.2670G>A
|
|
|
NR_138149.2:n.2754G>A
|
|
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