ENST00000366930.9:c.*205G>A
MANE Select
|
ENSP00000355897.4:n.*205G>A
|
|
ENST00000366929.4:c.*205G>A
|
ENSP00000355896.4:n.*205G>A
|
|
ENST00000366930.8:c.*205G>A
|
ENSP00000355897.4:n.*205G>A
|
|
ENST00000479322.1:n.934G>A
|
|
|
NM_001135599.2:c.*205G>A
|
NP_001129071.1:n.*205G>A
|
|
NM_003238.3:c.*205G>A
|
NP_003229.1:n.*205G>A
|
|
NM_001135599.3:c.*205G>A
|
NP_001129071.1:n.*205G>A
|
|
NM_003238.4:c.*205G>A
|
NP_003229.1:n.*205G>A
|
|
NR_138148.1:n.2753G>A
|
|
|
NR_138149.1:n.2837G>A
|
|
|
NM_003238.5:c.*205G>A
|
NP_003229.1:n.*205G>A
|
|
NM_003238.6:c.*205G>A
MANE Select
|
NP_003229.1:n.*205G>A
|
|
NM_001135599.4:c.*205G>A
|
NP_001129071.1:n.*205G>A
|
|
NR_138148.2:n.2701G>A
|
|
|
NR_138149.2:n.2785G>A
|
|
|