|
ENST00000415928.6:c.894-291C>G
|
ENSP00000388838.2:n.894-291C>G
|
|
|
ENST00000435065.7:c.1125-291C>G
|
ENSP00000402760.2:n.1125-291C>G
|
|
|
ENST00000448810.6:c.1053-377C>G
|
ENSP00000401860.2:n.1053-377C>G
|
|
|
ENST00000685543.1:n.1194-291C>G
|
|
|
|
ENST00000686757.1:c.*217-291C>G
|
ENSP00000510721.1:n.*217-291C>G
|
|
|
ENST00000687740.1:n.3738-291C>G
|
|
|
|
ENST00000688151.1:n.2363-291C>G
|
|
|
|
ENST00000689271.1:c.900-291C>G
|
ENSP00000510797.1:n.900-291C>G
|
|
|
ENST00000690900.1:c.*217-291C>G
|
ENSP00000510703.1:n.*217-291C>G
|
|
|
ENST00000692212.1:n.2374C>G
|
|
|
|
ENST00000692355.1:c.306-291C>G
|
|
|
|
ENST00000692413.1:c.1035-291C>G
|
ENSP00000509374.1:n.1035-291C>G
|
|
|
ENST00000692825.1:c.1121-291C>G
|
ENSP00000509447.1:n.1121-291C>G
|
|
|
ENST00000693308.1:c.1101-291C>G
|
ENSP00000509770.1:n.1101-291C>G
|
|
|
ENST00000693763.1:n.2213-291C>G
|
|
|
|
ENST00000245407.8:c.1053-291C>G
MANE Select
|
ENSP00000245407.3:n.1053-291C>G
|
|
|
ENST00000245407.7:c.1053-291C>G
|
ENSP00000245407.3:n.1053-291C>G
|
|
|
ENST00000435065.6:c.1125-291C>G
|
ENSP00000402760.2:n.1125-291C>G
|
|
|
ENST00000447841.5:c.111+1378C>G
|
|
|
|
ENST00000448810.5:c.401-377C>G
|
|
|
|
ENST00000461013.5:n.8475-291C>G
|
|
|
|
ENST00000475308.1:n.1440C>G
|
|
|
|
ENST00000479605.5:n.156-291C>G
|
|
|
|
NM_001308122.1:c.1125-291C>G
|
NP_001295051.1:n.1125-291C>G
|
|
|
NM_003060.3:c.1053-291C>G
|
NP_003051.1:n.1053-291C>G
|
|
|
XM_011543590.1:c.435-291C>G
|
XP_011541892.1:n.435-291C>G
|
|
|
XR_427718.1:n.1413-291C>G
|
|
|
|
XR_948290.1:n.1393+1378C>G
|
|
|
|
XR_948291.1:n.1407-291C>G
|
|
|
|
XM_011543590.2:c.435-291C>G
|
XP_011541892.1:n.435-291C>G
|
|
|
XM_017009778.2:c.525-291C>G
|
XP_016865267.1:n.525-291C>G
|
|
|
XR_001742215.1:n.1394-377C>G
|
|
|
|
XR_001742216.1:n.1413-377C>G
|
|
|
|
XR_427718.2:n.1413-291C>G
|
|
|
|
XR_948290.2:n.1393+1378C>G
|
|
|
|
XR_948291.2:n.1407-291C>G
|
|
|
|
NM_003060.4:c.1053-291C>G
MANE Select
|
NP_003051.1:n.1053-291C>G
|
|
|
NM_001308122.2:c.1125-291C>G
|
NP_001295051.1:n.1125-291C>G
|
|
