|
ENST00000415928.6:c.1010C>T
|
ENSP00000388838.2:p.Ala337Val
|
|
|
ENST00000435065.7:c.1241C>T
|
ENSP00000402760.2:p.Ala414Val
|
|
|
ENST00000448810.6:c.*21C>T
|
ENSP00000401860.2:n.*21C>T
|
|
|
ENST00000685543.1:n.1310C>T
|
|
|
|
ENST00000686757.1:c.*333C>T
|
ENSP00000510721.1:n.*333C>T
|
|
|
ENST00000687740.1:n.3854C>T
|
|
|
|
ENST00000688151.1:n.2479C>T
|
|
|
|
ENST00000689271.1:c.1016C>T
|
ENSP00000510797.1:p.Ala339Val
|
|
|
ENST00000690900.1:c.*333C>T
|
ENSP00000510703.1:n.*333C>T
|
|
|
ENST00000692212.1:n.2781C>T
|
|
|
|
ENST00000692355.1:c.422C>T
|
|
|
|
ENST00000692413.1:c.1151C>T
|
ENSP00000509374.1:p.Ala384Val
|
|
|
ENST00000692825.1:c.1237C>T
|
ENSP00000509447.1:n.1237C>T
|
|
|
ENST00000693308.1:c.1217C>T
|
ENSP00000509770.1:p.Ala406Val
|
|
|
ENST00000693763.1:n.2329C>T
|
|
|
|
ENST00000245407.8:c.1169C>T
MANE Select
|
ENSP00000245407.3:p.Ala390Val
|
|
|
ENST00000245407.7:c.1169C>T
|
ENSP00000245407.3:p.Ala390Val
|
|
|
ENST00000435065.6:c.1241C>T
|
ENSP00000402760.2:p.Ala414Val
|
|
|
ENST00000447841.5:c.112-1627C>T
|
|
|
|
ENST00000448810.5:c.431C>T
|
|
|
|
ENST00000461013.5:n.8591C>T
|
|
|
|
ENST00000475308.1:n.1847C>T
|
|
|
|
ENST00000479605.5:n.272C>T
|
|
|
|
NM_001308122.1:c.1241C>T
|
NP_001295051.1:p.Ala414Val
|
|
|
NM_003060.3:c.1169C>T
|
NP_003051.1:p.Ala390Val
|
|
|
XM_011543590.1:c.551C>T
|
XP_011541892.1:p.Ala184Val
|
|
|
XR_427718.1:n.1529C>T
|
|
|
|
XR_948290.1:n.1394-1627C>T
|
|
|
|
XR_948291.1:n.1523C>T
|
|
|
|
XM_011543590.2:c.551C>T
|
XP_011541892.1:p.Ala184Val
|
|
|
XM_017009778.2:c.641C>T
|
XP_016865267.1:p.Ala214Val
|
|
|
XR_001742215.1:n.1424C>T
|
|
|
|
XR_001742216.1:n.1443C>T
|
|
|
|
XR_427718.2:n.1529C>T
|
|
|
|
XR_948290.2:n.1394-1627C>T
|
|
|
|
XR_948291.2:n.1523C>T
|
|
|
|
NM_003060.4:c.1169C>T
MANE Select
|
NP_003051.1:p.Ala390Val
|
|
|
NM_001308122.2:c.1241C>T
|
NP_001295051.1:p.Ala414Val
|
|
