ENST00000227322.8:c.424+124G>T
MANE Select
|
ENSP00000227322.3:n.424+124G>T
|
|
ENST00000227322.7:c.424+124G>T
|
ENSP00000227322.3:n.424+124G>T
|
|
ENST00000425791.1:c.*246+124G>T
|
ENSP00000410141.1:n.*246+124G>T
|
|
ENST00000429220.5:c.251+124G>T
|
|
|
ENST00000431973.5:c.291+124G>T
|
|
|
ENST00000444935.5:c.423+124G>T
|
|
|
ENST00000498065.1:n.368+124G>T
|
|
|
NM_003904.3:c.424+124G>T
|
NP_003895.1:n.424+124G>T
|
|
NM_001317086.1:c.262+124G>T
|
NP_001304015.1:n.262+124G>T
|
|
NM_003904.4:c.424+124G>T
|
NP_003895.1:n.424+124G>T
|
|
XR_001748023.2:n.1706+124G>T
|
|
|
NM_003904.5:c.424+124G>T
MANE Select
|
NP_003895.1:n.424+124G>T
|
|
NM_001317086.2:c.262+124G>T
|
NP_001304015.1:n.262+124G>T
|
|