|
ENST00000415928.6:c.1084C>G
|
ENSP00000388838.2:p.Leu362Val
|
|
|
ENST00000435065.7:c.1315C>G
|
ENSP00000402760.2:p.Leu439Val
|
|
|
ENST00000448810.6:c.*95C>G
|
ENSP00000401860.2:n.*95C>G
|
|
|
ENST00000685543.1:n.1384C>G
|
|
|
|
ENST00000686757.1:c.*407C>G
|
ENSP00000510721.1:n.*407C>G
|
|
|
ENST00000687740.1:n.3928C>G
|
|
|
|
ENST00000688151.1:n.2553C>G
|
|
|
|
ENST00000689271.1:c.1090C>G
|
ENSP00000510797.1:p.Leu364Val
|
|
|
ENST00000690900.1:c.*407C>G
|
ENSP00000510703.1:n.*407C>G
|
|
|
ENST00000692212.1:n.2855C>G
|
|
|
|
ENST00000692355.1:c.496C>G
|
|
|
|
ENST00000692413.1:c.1225C>G
|
ENSP00000509374.1:p.Leu409Val
|
|
|
ENST00000692825.1:c.1311C>G
|
ENSP00000509447.1:n.1311C>G
|
|
|
ENST00000693308.1:c.1291C>G
|
ENSP00000509770.1:p.Leu431Val
|
|
|
ENST00000693763.1:n.2403C>G
|
|
|
|
ENST00000245407.8:c.1243C>G
MANE Select
|
ENSP00000245407.3:p.Leu415Val
|
|
|
ENST00000245407.7:c.1243C>G
|
ENSP00000245407.3:p.Leu415Val
|
|
|
ENST00000435065.6:c.1315C>G
|
ENSP00000402760.2:p.Leu439Val
|
|
|
ENST00000447841.5:c.112-1553C>G
|
|
|
|
ENST00000448810.5:c.505C>G
|
|
|
|
ENST00000461013.5:n.8665C>G
|
|
|
|
ENST00000475308.1:n.1921C>G
|
|
|
|
ENST00000479605.5:n.346C>G
|
|
|
|
NM_001308122.1:c.1315C>G
|
NP_001295051.1:p.Leu439Val
|
|
|
NM_003060.3:c.1243C>G
|
NP_003051.1:p.Leu415Val
|
|
|
XM_011543590.1:c.625C>G
|
XP_011541892.1:p.Leu209Val
|
|
|
XR_427718.1:n.1603C>G
|
|
|
|
XR_948290.1:n.1394-1553C>G
|
|
|
|
XR_948291.1:n.1597C>G
|
|
|
|
XM_011543590.2:c.625C>G
|
XP_011541892.1:p.Leu209Val
|
|
|
XM_017009778.2:c.715C>G
|
XP_016865267.1:p.Leu239Val
|
|
|
XR_001742215.1:n.1498C>G
|
|
|
|
XR_001742216.1:n.1517C>G
|
|
|
|
XR_427718.2:n.1603C>G
|
|
|
|
XR_948290.2:n.1394-1553C>G
|
|
|
|
XR_948291.2:n.1597C>G
|
|
|
|
NM_003060.4:c.1243C>G
MANE Select
|
NP_003051.1:p.Leu415Val
|
|
|
NM_001308122.2:c.1315C>G
|
NP_001295051.1:p.Leu439Val
|
|
