ENST00000415928.6:c.1076G>C
|
ENSP00000388838.2:p.Ser359Thr
|
|
ENST00000435065.7:c.1307G>C
|
ENSP00000402760.2:p.Ser436Thr
|
|
ENST00000448810.6:c.*87G>C
|
ENSP00000401860.2:n.*87G>C
|
|
ENST00000685543.1:n.1376G>C
|
|
|
ENST00000686757.1:c.*399G>C
|
ENSP00000510721.1:n.*399G>C
|
|
ENST00000687740.1:n.3920G>C
|
|
|
ENST00000688151.1:n.2545G>C
|
|
|
ENST00000689271.1:c.1082G>C
|
ENSP00000510797.1:p.Ser361Thr
|
|
ENST00000690900.1:c.*399G>C
|
ENSP00000510703.1:n.*399G>C
|
|
ENST00000692212.1:n.2847G>C
|
|
|
ENST00000692355.1:c.488G>C
|
|
|
ENST00000692413.1:c.1217G>C
|
ENSP00000509374.1:p.Ser406Thr
|
|
ENST00000692825.1:c.1303G>C
|
ENSP00000509447.1:n.1303G>C
|
|
ENST00000693308.1:c.1283G>C
|
ENSP00000509770.1:p.Ser428Thr
|
|
ENST00000693763.1:n.2395G>C
|
|
|
ENST00000245407.8:c.1235G>C
MANE Select
|
ENSP00000245407.3:p.Ser412Thr
|
|
ENST00000245407.7:c.1235G>C
|
ENSP00000245407.3:p.Ser412Thr
|
|
ENST00000435065.6:c.1307G>C
|
ENSP00000402760.2:p.Ser436Thr
|
|
ENST00000447841.5:c.112-1561G>C
|
|
|
ENST00000448810.5:c.497G>C
|
|
|
ENST00000461013.5:n.8657G>C
|
|
|
ENST00000475308.1:n.1913G>C
|
|
|
ENST00000479605.5:n.338G>C
|
|
|
NM_001308122.1:c.1307G>C
|
NP_001295051.1:p.Ser436Thr
|
|
NM_003060.3:c.1235G>C
|
NP_003051.1:p.Ser412Thr
|
|
XM_011543590.1:c.617G>C
|
XP_011541892.1:p.Ser206Thr
|
|
XR_427718.1:n.1595G>C
|
|
|
XR_948290.1:n.1394-1561G>C
|
|
|
XR_948291.1:n.1589G>C
|
|
|
XM_011543590.2:c.617G>C
|
XP_011541892.1:p.Ser206Thr
|
|
XM_017009778.2:c.707G>C
|
XP_016865267.1:p.Ser236Thr
|
|
XR_001742215.1:n.1490G>C
|
|
|
XR_001742216.1:n.1509G>C
|
|
|
XR_427718.2:n.1595G>C
|
|
|
XR_948290.2:n.1394-1561G>C
|
|
|
XR_948291.2:n.1589G>C
|
|
|
NM_003060.4:c.1235G>C
MANE Select
|
NP_003051.1:p.Ser412Thr
|
|
NM_001308122.2:c.1307G>C
|
NP_001295051.1:p.Ser436Thr
|
|