|
ENST00000415928.6:c.1108+22G>T
|
ENSP00000388838.2:n.1108+22G>T
|
|
|
ENST00000435065.7:c.1339+22G>T
|
ENSP00000402760.2:n.1339+22G>T
|
|
|
ENST00000448810.6:c.*119+22G>T
|
ENSP00000401860.2:n.*119+22G>T
|
|
|
ENST00000685543.1:n.1408+22G>T
|
|
|
|
ENST00000686757.1:c.*431+22G>T
|
ENSP00000510721.1:n.*431+22G>T
|
|
|
ENST00000687740.1:n.3952+22G>T
|
|
|
|
ENST00000688151.1:n.2577+22G>T
|
|
|
|
ENST00000689271.1:c.1114+22G>T
|
ENSP00000510797.1:n.1114+22G>T
|
|
|
ENST00000690900.1:c.*431+22G>T
|
ENSP00000510703.1:n.*431+22G>T
|
|
|
ENST00000692212.1:n.2901G>T
|
|
|
|
ENST00000692355.1:c.520+22G>T
|
|
|
|
ENST00000692413.1:c.1249+22G>T
|
ENSP00000509374.1:n.1249+22G>T
|
|
|
ENST00000692825.1:c.1335+22G>T
|
ENSP00000509447.1:n.1335+22G>T
|
|
|
ENST00000693308.1:c.1315+22G>T
|
ENSP00000509770.1:n.1315+22G>T
|
|
|
ENST00000693763.1:n.2427+22G>T
|
|
|
|
ENST00000245407.8:c.1267+22G>T
MANE Select
|
ENSP00000245407.3:n.1267+22G>T
|
|
|
ENST00000245407.7:c.1267+22G>T
|
ENSP00000245407.3:n.1267+22G>T
|
|
|
ENST00000435065.6:c.1339+22G>T
|
ENSP00000402760.2:n.1339+22G>T
|
|
|
ENST00000447841.5:c.112-1507G>T
|
|
|
|
ENST00000448810.5:c.529+22G>T
|
|
|
|
ENST00000461013.5:n.8689+22G>T
|
|
|
|
ENST00000475308.1:n.1945+22G>T
|
|
|
|
ENST00000479605.5:n.370+22G>T
|
|
|
|
NM_001308122.1:c.1339+22G>T
|
NP_001295051.1:n.1339+22G>T
|
|
|
NM_003060.3:c.1267+22G>T
|
NP_003051.1:n.1267+22G>T
|
|
|
XM_011543590.1:c.649+22G>T
|
XP_011541892.1:n.649+22G>T
|
|
|
XR_427718.1:n.1627+22G>T
|
|
|
|
XR_948290.1:n.1394-1507G>T
|
|
|
|
XR_948291.1:n.1621+22G>T
|
|
|
|
XM_011543590.2:c.649+22G>T
|
XP_011541892.1:n.649+22G>T
|
|
|
XM_017009778.2:c.739+22G>T
|
XP_016865267.1:n.739+22G>T
|
|
|
XR_001742215.1:n.1522+22G>T
|
|
|
|
XR_001742216.1:n.1541+22G>T
|
|
|
|
XR_427718.2:n.1627+22G>T
|
|
|
|
XR_948290.2:n.1394-1507G>T
|
|
|
|
XR_948291.2:n.1621+22G>T
|
|
|
|
NM_003060.4:c.1267+22G>T
MANE Select
|
NP_003051.1:n.1267+22G>T
|
|
|
NM_001308122.2:c.1339+22G>T
|
NP_001295051.1:n.1339+22G>T
|
|
