|
ENST00000700029.2:c.1048A>T
|
ENSP00000514759.2:p.Thr350Ser
|
|
|
ENST00000710265.1:c.955A>T
|
ENSP00000518161.1:p.Thr319Ser
|
|
|
ENST00000472832.3:c.955A>T
|
ENSP00000483066.2:p.Thr319Ser
|
|
|
ENST00000688158.2:n.1690A>T
|
|
|
|
ENST00000688922.2:c.*785A>T
|
ENSP00000508742.2:n.*785A>T
|
|
|
ENST00000700021.1:c.910A>T
|
ENSP00000514757.1:p.Thr304Ser
|
|
|
ENST00000700022.1:c.*294A>T
|
ENSP00000514758.1:n.*294A>T
|
|
|
ENST00000700023.1:n.2113A>T
|
|
|
|
ENST00000700024.1:n.2347A>T
|
|
|
|
ENST00000700025.1:n.1724A>T
|
|
|
|
ENST00000700026.1:n.592A>T
|
|
|
|
ENST00000706954.1:c.955A>T
|
ENSP00000516674.1:p.Thr319Ser
|
|
|
ENST00000706955.1:c.*990A>T
|
ENSP00000516675.1:n.*990A>T
|
|
|
ENST00000686459.1:c.*541A>T
|
ENSP00000508909.1:n.*541A>T
|
|
|
ENST00000688158.1:c.*1066A>T
|
ENSP00000509254.1:n.*1066A>T
|
|
|
ENST00000688308.1:c.955A>T
|
ENSP00000508752.1:p.Thr319Ser
|
|
|
ENST00000688922.1:c.876A>T
|
|
|
|
ENST00000693560.1:c.1474A>T
|
ENSP00000509861.1:p.Thr492Ser
|
|
|
ENST00000371953.8:c.955A>T
MANE Select
|
ENSP00000361021.3:p.Thr319Ser
|
|
|
ENST00000371953.7:c.955A>T
|
ENSP00000361021.3:p.Thr319Ser
|
|
|
ENST00000472832.2:c.382A>T
|
ENSP00000483066.1:p.Thr128Ser
|
|
|
NM_000314.5:c.955A>T
|
NP_000305.3:p.Thr319Ser
|
|
|
NM_000314.6:c.955A>T
|
NP_000305.3:p.Thr319Ser
|
|
|
NM_001304717.2:c.1474A>T
|
NP_001291646.2:p.Thr492Ser
|
|
|
NM_001304718.1:c.364A>T
|
NP_001291647.1:p.Thr122Ser
|
|
|
XM_006717926.2:c.910A>T
|
XP_006717989.1:p.Thr304Ser
|
|
|
XM_011539981.1:c.955A>T
|
XP_011538283.1:p.Thr319Ser
|
|
|
XM_011539982.1:c.859A>T
|
XP_011538284.1:p.Thr287Ser
|
|
|
XR_945791.1:n.1525A>T
|
|
|
|
NM_000314.7:c.955A>T
|
NP_000305.3:p.Thr319Ser
|
|
|
NM_001304717.5:c.1474A>T
|
NP_001291646.4:p.Thr492Ser
|
|
|
NM_001304718.2:c.364A>T
|
NP_001291647.1:p.Thr122Ser
|
|
|
NM_000314.8:c.955A>T
MANE Select
|
NP_000305.3:p.Thr319Ser
|
|
