|
ENST00000415928.6:c.1109-37G>T
|
ENSP00000388838.2:n.1109-37G>T
|
|
|
ENST00000435065.7:c.1340-37G>T
|
ENSP00000402760.2:n.1340-37G>T
|
|
|
ENST00000448810.6:c.*120-37G>T
|
ENSP00000401860.2:n.*120-37G>T
|
|
|
ENST00000685543.1:n.1409-37G>T
|
|
|
|
ENST00000686757.1:c.*432-37G>T
|
ENSP00000510721.1:n.*432-37G>T
|
|
|
ENST00000687740.1:n.3953-37G>T
|
|
|
|
ENST00000688151.1:n.2578-37G>T
|
|
|
|
ENST00000689271.1:c.1115-37G>T
|
ENSP00000510797.1:n.1115-37G>T
|
|
|
ENST00000690900.1:c.*432-37G>T
|
ENSP00000510703.1:n.*432-37G>T
|
|
|
ENST00000692212.1:n.4371G>T
|
|
|
|
ENST00000692355.1:c.521-37G>T
|
|
|
|
ENST00000692413.1:c.1250-37G>T
|
ENSP00000509374.1:n.1250-37G>T
|
|
|
ENST00000692825.1:c.1336-37G>T
|
ENSP00000509447.1:n.1336-37G>T
|
|
|
ENST00000693308.1:c.1316-37G>T
|
ENSP00000509770.1:n.1316-37G>T
|
|
|
ENST00000693763.1:n.2428-37G>T
|
|
|
|
ENST00000245407.8:c.1268-37G>T
MANE Select
|
ENSP00000245407.3:n.1268-37G>T
|
|
|
ENST00000245407.7:c.1268-37G>T
|
ENSP00000245407.3:n.1268-37G>T
|
|
|
ENST00000435065.6:c.1340-37G>T
|
ENSP00000402760.2:n.1340-37G>T
|
|
|
ENST00000447841.5:c.112-37G>T
|
|
|
|
ENST00000448810.5:c.530-37G>T
|
|
|
|
ENST00000461013.5:n.8690-37G>T
|
|
|
|
ENST00000475308.1:n.1946-37G>T
|
|
|
|
ENST00000479605.5:n.371-37G>T
|
|
|
|
NM_001308122.1:c.1340-37G>T
|
NP_001295051.1:n.1340-37G>T
|
|
|
NM_003060.3:c.1268-37G>T
|
NP_003051.1:n.1268-37G>T
|
|
|
XM_011543590.1:c.650-37G>T
|
XP_011541892.1:n.650-37G>T
|
|
|
XR_427718.1:n.1628-37G>T
|
|
|
|
XR_948290.1:n.1394-37G>T
|
|
|
|
XR_948291.1:n.1622-37G>T
|
|
|
|
XM_011543590.2:c.650-37G>T
|
XP_011541892.1:n.650-37G>T
|
|
|
XM_017009778.2:c.740-37G>T
|
XP_016865267.1:n.740-37G>T
|
|
|
XR_001742215.1:n.1523-37G>T
|
|
|
|
XR_001742216.1:n.1542-37G>T
|
|
|
|
XR_427718.2:n.1628-37G>T
|
|
|
|
XR_948290.2:n.1394-37G>T
|
|
|
|
XR_948291.2:n.1622-37G>T
|
|
|
|
NM_003060.4:c.1268-37G>T
MANE Select
|
NP_003051.1:n.1268-37G>T
|
|
|
NM_001308122.2:c.1340-37G>T
|
NP_001295051.1:n.1340-37G>T
|
|
