|
ENST00000284995.11:c.1387G>T
(TSEN2)
MANE Select
|
ENSP00000284995.6:p.Asp463Tyr
|
|
|
ENST00000412698.3:c.1260+1051G>T
(TSEN2)
|
ENSP00000408528.3:n.1260+1051G>T
|
|
|
ENST00000415684.6:c.1309G>T
(TSEN2)
|
ENSP00000416510.1:p.Asp437Tyr
|
|
|
ENST00000444864.6:c.1260+1051G>T
(TSEN2)
|
ENSP00000407974.2:n.1260+1051G>T
|
|
|
ENST00000446004.6:c.1338+1051G>T
(TSEN2)
|
ENSP00000406238.2:n.1338+1051G>T
|
|
|
ENST00000455118.6:c.*228G>T
(TSEN2)
|
ENSP00000408744.2:n.*228G>T
|
|
|
ENST00000475595.2:n.4070G>T
(TSEN2)
|
|
|
|
ENST00000679367.1:c.*1006G>T
(TSEN2)
|
ENSP00000506510.1:n.*1006G>T
|
|
|
ENST00000679420.1:n.1560G>T
(TSEN2)
|
|
|
|
ENST00000679424.1:c.*1230G>T
(TSEN2)
|
ENSP00000505917.1:n.*1230G>T
|
|
|
ENST00000679425.1:c.1387G>T
(TSEN2)
|
ENSP00000505890.1:p.Asp463Tyr
|
|
|
ENST00000679492.1:c.1338+1051G>T
(TSEN2)
|
ENSP00000505331.1:n.1338+1051G>T
|
|
|
ENST00000679555.1:c.*1110G>T
(TSEN2)
|
ENSP00000505538.1:n.*1110G>T
|
|
|
ENST00000679670.1:c.1309G>T
(TSEN2)
|
ENSP00000506080.1:p.Asp437Tyr
|
|
|
ENST00000679690.1:c.*386G>T
(TSEN2)
|
ENSP00000506383.1:n.*386G>T
|
|
|
ENST00000679693.1:c.*175+1051G>T
(TSEN2)
|
ENSP00000505108.1:n.*175+1051G>T
|
|
|
ENST00000679699.1:c.1387G>T
(TSEN2)
|
ENSP00000505274.1:p.Asp463Tyr
|
|
|
ENST00000679756.1:c.1336G>T
(TSEN2)
|
ENSP00000506391.1:p.Asp446Tyr
|
|
|
ENST00000679785.1:c.*228G>T
(TSEN2)
|
ENSP00000506473.1:n.*228G>T
|
|
|
ENST00000679835.1:c.*576G>T
(TSEN2)
|
ENSP00000505616.1:n.*576G>T
|
|
|
ENST00000679876.1:c.1209+1051G>T
(TSEN2)
|
ENSP00000504930.1:n.1209+1051G>T
|
|
|
ENST00000679995.1:c.*228G>T
(TSEN2)
|
ENSP00000505221.1:n.*228G>T
|
|
|
ENST00000680126.1:c.*1226G>T
(TSEN2)
|
ENSP00000505345.1:n.*1226G>T
|
|
|
ENST00000680264.1:c.*527+1051G>T
(TSEN2)
|
ENSP00000505273.1:n.*527+1051G>T
|
|
|
ENST00000680275.1:c.1444G>T
(TSEN2)
|
ENSP00000505417.1:p.Asp482Tyr
|
|
|
ENST00000680354.1:c.1366G>T
(TSEN2)
|
ENSP00000505106.1:p.Asp456Tyr
|
|
|
ENST00000680376.1:c.*576G>T
(TSEN2)
|
ENSP00000506369.1:n.*576G>T
|
|
|
ENST00000680421.1:c.1258G>T
(TSEN2)
|
ENSP00000505530.1:p.Asp420Tyr
|
|
|
ENST00000680449.1:c.*529G>T
(TSEN2)
|
ENSP00000505709.1:n.*529G>T
|
|
|
ENST00000680458.1:c.*202G>T
(TSEN2)
|
ENSP00000505979.1:n.*202G>T
|
|
|
ENST00000680555.1:c.*228G>T
(TSEN2)
|
ENSP00000505160.1:n.*228G>T
|
|
|
ENST00000680598.1:c.1336G>T
(TSEN2)
|
ENSP00000506297.1:p.Asp446Tyr
|
|
|
ENST00000680765.1:c.*228G>T
(TSEN2)
|
ENSP00000505351.1:n.*228G>T
|
|
|
ENST00000680817.1:c.1258G>T
(TSEN2)
|
ENSP00000506221.1:p.Asp420Tyr
|
|
|
ENST00000680857.1:c.1338+1051G>T
(TSEN2)
|
ENSP00000506578.1:n.1338+1051G>T
|
|
|
ENST00000680873.1:c.*539G>T
(TSEN2)
|
ENSP00000505233.1:n.*539G>T
|
|
|
ENST00000680923.1:c.*576G>T
(TSEN2)
|
ENSP00000505344.1:n.*576G>T
|
|
|
ENST00000680943.1:c.1336G>T
(TSEN2)
|
ENSP00000505442.1:p.Asp446Tyr
|
|
|
ENST00000680986.1:c.1387G>T
(TSEN2)
|
ENSP00000505799.1:p.Asp463Tyr
|
|
|
ENST00000681042.1:c.1100-6451G>T
(TSEN2)
|
ENSP00000505622.1:n.1100-6451G>T
|
|
|
ENST00000681073.1:c.*228G>T
(TSEN2)
|
ENSP00000506576.1:n.*228G>T
|
|
|
ENST00000681140.1:c.1387G>T
(TSEN2)
|
ENSP00000505099.1:p.Asp463Tyr
|
|
|
ENST00000681227.1:c.*259G>T
(TSEN2)
|
ENSP00000505240.1:n.*259G>T
|
|
|
ENST00000681268.1:c.*1531G>T
(TSEN2)
|
ENSP00000505385.1:n.*1531G>T
|
|
|
ENST00000681343.1:c.*1006G>T
(TSEN2)
|
ENSP00000506265.1:n.*1006G>T
|
|
|
ENST00000681433.1:c.*228G>T
(TSEN2)
|
ENSP00000505729.1:n.*228G>T
|
|
|
ENST00000681471.1:c.1309G>T
(TSEN2)
|
ENSP00000505105.1:p.Asp437Tyr
|
|
|
ENST00000681482.1:c.1387G>T
(TSEN2)
|
ENSP00000505436.1:p.Asp463Tyr
|
|
|
ENST00000681676.1:c.1309G>T
(TSEN2)
|
ENSP00000506163.1:p.Asp437Tyr
|
|
|
ENST00000681713.1:c.*1006G>T
(TSEN2)
|
ENSP00000506046.1:n.*1006G>T
|
|
|
ENST00000284995.10:c.1387G>T
(TSEN2)
|
ENSP00000284995.6:p.Asp463Tyr
|
|
|
ENST00000402228.7:c.1387G>T
(TSEN2)
|
ENSP00000385976.3:p.Asp463Tyr
|
|
|
ENST00000412698.2:c.93+1051G>T
(TSEN2)
|
ENSP00000408528.2:n.93+1051G>T
|
|
|
ENST00000415684.5:c.1309G>T
(TSEN2)
|
ENSP00000416510.1:p.Asp437Tyr
|
|
|
ENST00000454502.6:c.1210G>T
(TSEN2)
|
ENSP00000392029.2:p.Asp404Tyr
|
|
|
ENST00000455118.5:c.234G>T
(TSEN2)
|
|
|
|
ENST00000473755.5:n.3392G>T
(TSEN2)
|
|
|
|
ENST00000475595.1:n.233G>T
(TSEN2)
|
|
|
|
ENST00000567514.1:n.715+6797C>A
(MKRN2OS)
|
|
|
|
NM_001145392.1:c.1387G>T
(TSEN2)
|
NP_001138864.1:p.Asp463Tyr
|
|
|
NM_001145393.1:c.1309G>T
(TSEN2)
|
NP_001138865.1:p.Asp437Tyr
|
|
|
NM_001145394.1:c.1210G>T
(TSEN2)
|
NP_001138866.1:p.Asp404Tyr
|
|
|
NM_025265.3:c.1387G>T
(TSEN2)
|
NP_079541.1:p.Asp463Tyr
|
|
|
XM_005265495.1:c.1387G>T
(TSEN2)
|
XP_005265552.1:p.Asp463Tyr
|
|
|
XM_005265497.1:c.1309G>T
(TSEN2)
|
XP_005265554.1:p.Asp437Tyr
|
|
|
XM_005265498.1:c.1258G>T
(TSEN2)
|
XP_005265555.1:p.Asp420Tyr
|
|
|
XM_011534138.1:c.1120G>T
(TSEN2)
|
XP_011532440.1:p.Asp374Tyr
|
|
|
XM_011534139.1:c.1114G>T
(TSEN2)
|
XP_011532441.1:p.Asp372Tyr
|
|
|
XR_245158.1:n.1490G>T
(TSEN2)
|
|
|
|
XR_245159.3:n.1490G>T
(TSEN2)
|
|
|
|
XR_427295.2:n.3392G>T
(TSEN2)
|
|
|
|
XR_427296.1:n.1300G>T
(TSEN2)
|
|
|
|
NM_001145393.2:c.1309G>T
(TSEN2)
|
NP_001138865.1:p.Asp437Tyr
|
|
|
NM_001321277.1:c.1387G>T
(TSEN2)
|
NP_001308206.1:p.Asp463Tyr
|
|
|
NM_001321278.1:c.1338+1051G>T
(TSEN2)
|
NP_001308207.1:n.1338+1051G>T
|
|
|
NM_001321279.1:c.1309G>T
(TSEN2)
|
NP_001308208.1:p.Asp437Tyr
|
|
|
NR_135607.1:n.1490G>T
(TSEN2)
|
|
|
|
XM_011534139.3:c.1114G>T
(TSEN2)
|
XP_011532441.1:p.Asp372Tyr
|
|
|
XM_017007292.1:c.1444G>T
(TSEN2)
|
XP_016862781.1:p.Asp482Tyr
|
|
|
XM_017007293.1:c.1444G>T
(TSEN2)
|
XP_016862782.1:p.Asp482Tyr
|
|
|
XM_017007294.1:c.1444G>T
(TSEN2)
|
XP_016862783.1:p.Asp482Tyr
|
|
|
XM_017007295.2:c.1444G>T
(TSEN2)
|
XP_016862784.1:p.Asp482Tyr
|
|
|
XM_017007296.2:c.1387G>T
(TSEN2)
|
XP_016862785.1:p.Asp463Tyr
|
|
|
XM_017007297.1:c.1366G>T
(TSEN2)
|
XP_016862786.1:p.Asp456Tyr
|
|
|
XM_024453785.1:c.1309G>T
(TSEN2)
|
XP_024309553.1:p.Asp437Tyr
|
|
|
XR_001740287.1:n.1831G>T
(TSEN2)
|
|
|
|
XR_001740288.2:n.1831G>T
(TSEN2)
|
|
|
|
XR_001740289.2:n.1774G>T
(TSEN2)
|
|
|
|
XR_001740290.2:n.1388G>T
(TSEN2)
|
|
|
|
XR_001740291.1:n.1696G>T
(TSEN2)
|
|
|
|
XR_001740292.1:n.1794G>T
(TSEN2)
|
|
|
|
XR_001740293.1:n.1794G>T
(TSEN2)
|
|
|
|
XR_001740294.2:n.1429G>T
(TSEN2)
|
|
|
|
XR_001740295.2:n.1351G>T
(TSEN2)
|
|
|
|
XR_001740296.1:n.1641G>T
(TSEN2)
|
|
|
|
XR_001740297.1:n.1959G>T
(TSEN2)
|
|
|
|
XR_001740298.2:n.1276G>T
(TSEN2)
|
|
|
|
XR_001740300.2:n.1594G>T
(TSEN2)
|
|
|
|
XR_001740301.2:n.1594G>T
(TSEN2)
|
|
|
|
XR_001740302.2:n.1557G>T
(TSEN2)
|
|
|
|
XR_001740303.2:n.1404G>T
(TSEN2)
|
|
|
|
XR_001740304.1:n.1712G>T
(TSEN2)
|
|
|
|
XR_002959592.1:n.1565G>T
(TSEN2)
|
|
|
|
XR_002959593.1:n.1522G>T
(TSEN2)
|
|
|
|
XR_002959594.1:n.1562G>T
(TSEN2)
|
|
|
|
XR_002959595.1:n.1902G>T
(TSEN2)
|
|
|
|
XR_427296.2:n.1276G>T
(TSEN2)
|
|
|
|
NM_001321278.2:c.1338+1051G>T
(TSEN2)
|
NP_001308207.1:n.1338+1051G>T
|
|
|
NM_025265.4:c.1387G>T
(TSEN2)
MANE Select
|
NP_079541.1:p.Asp463Tyr
|
|
|
NR_135607.2:n.1442G>T
(TSEN2)
|
|
|
|
NM_001145392.2:c.1387G>T
(TSEN2)
|
NP_001138864.1:p.Asp463Tyr
|
|
|
NM_001145393.3:c.1309G>T
(TSEN2)
|
NP_001138865.1:p.Asp437Tyr
|
|
|
NM_001145394.2:c.1210G>T
(TSEN2)
|
NP_001138866.1:p.Asp404Tyr
|
|
|
NM_001321277.2:c.1387G>T
(TSEN2)
|
NP_001308206.1:p.Asp463Tyr
|
|
|
NM_001321279.2:c.1309G>T
(TSEN2)
|
NP_001308208.1:p.Asp437Tyr
|
|
