|
ENST00000415928.6:c.1105C>T
|
ENSP00000388838.2:p.Pro369Ser
|
|
|
ENST00000435065.7:c.1336C>T
|
ENSP00000402760.2:p.Pro446Ser
|
|
|
ENST00000448810.6:c.*116C>T
|
ENSP00000401860.2:n.*116C>T
|
|
|
ENST00000685543.1:n.1405C>T
|
|
|
|
ENST00000686757.1:c.*428C>T
|
ENSP00000510721.1:n.*428C>T
|
|
|
ENST00000687740.1:n.3949C>T
|
|
|
|
ENST00000688151.1:n.2574C>T
|
|
|
|
ENST00000689271.1:c.1111C>T
|
ENSP00000510797.1:p.Pro371Ser
|
|
|
ENST00000690900.1:c.*428C>T
|
ENSP00000510703.1:n.*428C>T
|
|
|
ENST00000692212.1:n.2876C>T
|
|
|
|
ENST00000692355.1:c.517C>T
|
|
|
|
ENST00000692413.1:c.1246C>T
|
ENSP00000509374.1:p.Pro416Ser
|
|
|
ENST00000692825.1:c.1332C>T
|
ENSP00000509447.1:n.1332C>T
|
|
|
ENST00000693308.1:c.1312C>T
|
ENSP00000509770.1:p.Pro438Ser
|
|
|
ENST00000693763.1:n.2424C>T
|
|
|
|
ENST00000245407.8:c.1264C>T
MANE Select
|
ENSP00000245407.3:p.Pro422Ser
|
|
|
ENST00000245407.7:c.1264C>T
|
ENSP00000245407.3:p.Pro422Ser
|
|
|
ENST00000435065.6:c.1336C>T
|
ENSP00000402760.2:p.Pro446Ser
|
|
|
ENST00000447841.5:c.112-1532C>T
|
|
|
|
ENST00000448810.5:c.526C>T
|
|
|
|
ENST00000461013.5:n.8686C>T
|
|
|
|
ENST00000475308.1:n.1942C>T
|
|
|
|
ENST00000479605.5:n.367C>T
|
|
|
|
NM_001308122.1:c.1336C>T
|
NP_001295051.1:p.Pro446Ser
|
|
|
NM_003060.3:c.1264C>T
|
NP_003051.1:p.Pro422Ser
|
|
|
XM_011543590.1:c.646C>T
|
XP_011541892.1:p.Pro216Ser
|
|
|
XR_427718.1:n.1624C>T
|
|
|
|
XR_948290.1:n.1394-1532C>T
|
|
|
|
XR_948291.1:n.1618C>T
|
|
|
|
XM_011543590.2:c.646C>T
|
XP_011541892.1:p.Pro216Ser
|
|
|
XM_017009778.2:c.736C>T
|
XP_016865267.1:p.Pro246Ser
|
|
|
XR_001742215.1:n.1519C>T
|
|
|
|
XR_001742216.1:n.1538C>T
|
|
|
|
XR_427718.2:n.1624C>T
|
|
|
|
XR_948290.2:n.1394-1532C>T
|
|
|
|
XR_948291.2:n.1618C>T
|
|
|
|
NM_003060.4:c.1264C>T
MANE Select
|
NP_003051.1:p.Pro422Ser
|
|
|
NM_001308122.2:c.1336C>T
|
NP_001295051.1:p.Pro446Ser
|
|
