ENST00000465459.2:c.403+2964G>T
(HLA-F)
|
ENSP00000486947.1:n.403+2964G>T
|
|
ENST00000475996.1:c.1161G>T
(HLA-F)
|
|
|
NR_026972.1:n.1236-512C>A
(HLA-F-AS1)
|
|
|
NR_026973.1:n.151-1868C>A
(HLA-F-AS1)
|
|
|
XM_011514563.1:c.1003+3444G>T
(HLA-F)
|
XP_011512865.1:n.1003+3444G>T
|
|
XM_011514564.1:c.1003+3444G>T
(HLA-F)
|
XP_011512866.1:n.1003+3444G>T
|
|
XM_017010810.1:c.*901G>T
(HLA-F)
|
XP_016866299.1:n.*901G>T
|
|
XM_017010813.1:c.1158+2003G>T
(HLA-F)
|
XP_016866302.1:n.1158+2003G>T
|
|
XR_001743373.1:n.1188+2003G>T
(HLA-F)
|
|
|
XR_001743374.1:n.1188+2003G>T
(HLA-F)
|
|
|
XR_001743376.1:n.1131+2003G>T
(HLA-F)
|
|
|