|
ENST00000284995.11:c.1381G>C
(TSEN2)
MANE Select
|
ENSP00000284995.6:p.Asp461His
|
|
|
ENST00000412698.3:c.1260+1045G>C
(TSEN2)
|
ENSP00000408528.3:n.1260+1045G>C
|
|
|
ENST00000415684.6:c.1303G>C
(TSEN2)
|
ENSP00000416510.1:p.Asp435His
|
|
|
ENST00000444864.6:c.1260+1045G>C
(TSEN2)
|
ENSP00000407974.2:n.1260+1045G>C
|
|
|
ENST00000446004.6:c.1338+1045G>C
(TSEN2)
|
ENSP00000406238.2:n.1338+1045G>C
|
|
|
ENST00000455118.6:c.*222G>C
(TSEN2)
|
ENSP00000408744.2:n.*222G>C
|
|
|
ENST00000475595.2:n.4064G>C
(TSEN2)
|
|
|
|
ENST00000679367.1:c.*1000G>C
(TSEN2)
|
ENSP00000506510.1:n.*1000G>C
|
|
|
ENST00000679420.1:n.1554G>C
(TSEN2)
|
|
|
|
ENST00000679424.1:c.*1224G>C
(TSEN2)
|
ENSP00000505917.1:n.*1224G>C
|
|
|
ENST00000679425.1:c.1381G>C
(TSEN2)
|
ENSP00000505890.1:p.Asp461His
|
|
|
ENST00000679492.1:c.1338+1045G>C
(TSEN2)
|
ENSP00000505331.1:n.1338+1045G>C
|
|
|
ENST00000679555.1:c.*1104G>C
(TSEN2)
|
ENSP00000505538.1:n.*1104G>C
|
|
|
ENST00000679670.1:c.1303G>C
(TSEN2)
|
ENSP00000506080.1:p.Asp435His
|
|
|
ENST00000679690.1:c.*380G>C
(TSEN2)
|
ENSP00000506383.1:n.*380G>C
|
|
|
ENST00000679693.1:c.*175+1045G>C
(TSEN2)
|
ENSP00000505108.1:n.*175+1045G>C
|
|
|
ENST00000679699.1:c.1381G>C
(TSEN2)
|
ENSP00000505274.1:p.Asp461His
|
|
|
ENST00000679756.1:c.1330G>C
(TSEN2)
|
ENSP00000506391.1:p.Asp444His
|
|
|
ENST00000679785.1:c.*222G>C
(TSEN2)
|
ENSP00000506473.1:n.*222G>C
|
|
|
ENST00000679835.1:c.*570G>C
(TSEN2)
|
ENSP00000505616.1:n.*570G>C
|
|
|
ENST00000679876.1:c.1209+1045G>C
(TSEN2)
|
ENSP00000504930.1:n.1209+1045G>C
|
|
|
ENST00000679995.1:c.*222G>C
(TSEN2)
|
ENSP00000505221.1:n.*222G>C
|
|
|
ENST00000680126.1:c.*1220G>C
(TSEN2)
|
ENSP00000505345.1:n.*1220G>C
|
|
|
ENST00000680264.1:c.*527+1045G>C
(TSEN2)
|
ENSP00000505273.1:n.*527+1045G>C
|
|
|
ENST00000680275.1:c.1438G>C
(TSEN2)
|
ENSP00000505417.1:p.Asp480His
|
|
|
ENST00000680354.1:c.1360G>C
(TSEN2)
|
ENSP00000505106.1:p.Asp454His
|
|
|
ENST00000680376.1:c.*570G>C
(TSEN2)
|
ENSP00000506369.1:n.*570G>C
|
|
|
ENST00000680421.1:c.1252G>C
(TSEN2)
|
ENSP00000505530.1:p.Asp418His
|
|
|
ENST00000680449.1:c.*523G>C
(TSEN2)
|
ENSP00000505709.1:n.*523G>C
|
|
|
ENST00000680458.1:c.*196G>C
(TSEN2)
|
ENSP00000505979.1:n.*196G>C
|
|
|
ENST00000680555.1:c.*222G>C
(TSEN2)
|
ENSP00000505160.1:n.*222G>C
|
|
|
ENST00000680598.1:c.1330G>C
(TSEN2)
|
ENSP00000506297.1:p.Asp444His
|
|
|
ENST00000680765.1:c.*222G>C
(TSEN2)
|
ENSP00000505351.1:n.*222G>C
|
|
|
ENST00000680817.1:c.1252G>C
(TSEN2)
|
ENSP00000506221.1:p.Asp418His
|
|
|
ENST00000680857.1:c.1338+1045G>C
(TSEN2)
|
ENSP00000506578.1:n.1338+1045G>C
|
|
|
ENST00000680873.1:c.*533G>C
(TSEN2)
|
ENSP00000505233.1:n.*533G>C
|
|
|
ENST00000680923.1:c.*570G>C
(TSEN2)
|
ENSP00000505344.1:n.*570G>C
|
|
|
ENST00000680943.1:c.1330G>C
(TSEN2)
|
ENSP00000505442.1:p.Asp444His
|
|
|
ENST00000680986.1:c.1381G>C
(TSEN2)
|
ENSP00000505799.1:p.Asp461His
|
|
|
ENST00000681042.1:c.1100-6457G>C
(TSEN2)
|
ENSP00000505622.1:n.1100-6457G>C
|
|
|
ENST00000681073.1:c.*222G>C
(TSEN2)
|
ENSP00000506576.1:n.*222G>C
|
|
|
ENST00000681140.1:c.1381G>C
(TSEN2)
|
ENSP00000505099.1:p.Asp461His
|
|
|
ENST00000681227.1:c.*253G>C
(TSEN2)
|
ENSP00000505240.1:n.*253G>C
|
|
|
ENST00000681268.1:c.*1525G>C
(TSEN2)
|
ENSP00000505385.1:n.*1525G>C
|
|
|
ENST00000681343.1:c.*1000G>C
(TSEN2)
|
ENSP00000506265.1:n.*1000G>C
|
|
|
ENST00000681433.1:c.*222G>C
(TSEN2)
|
ENSP00000505729.1:n.*222G>C
|
|
|
ENST00000681471.1:c.1303G>C
(TSEN2)
|
ENSP00000505105.1:p.Asp435His
|
|
|
ENST00000681482.1:c.1381G>C
(TSEN2)
|
ENSP00000505436.1:p.Asp461His
|
|
|
ENST00000681676.1:c.1303G>C
(TSEN2)
|
ENSP00000506163.1:p.Asp435His
|
|
|
ENST00000681713.1:c.*1000G>C
(TSEN2)
|
ENSP00000506046.1:n.*1000G>C
|
|
|
ENST00000284995.10:c.1381G>C
(TSEN2)
|
ENSP00000284995.6:p.Asp461His
|
|
|
ENST00000402228.7:c.1381G>C
(TSEN2)
|
ENSP00000385976.3:p.Asp461His
|
|
|
ENST00000412698.2:c.93+1045G>C
(TSEN2)
|
ENSP00000408528.2:n.93+1045G>C
|
|
|
ENST00000415684.5:c.1303G>C
(TSEN2)
|
ENSP00000416510.1:p.Asp435His
|
|
|
ENST00000454502.6:c.1204G>C
(TSEN2)
|
ENSP00000392029.2:p.Asp402His
|
|
|
ENST00000455118.5:c.228G>C
(TSEN2)
|
|
|
|
ENST00000473755.5:n.3386G>C
(TSEN2)
|
|
|
|
ENST00000475595.1:n.227G>C
(TSEN2)
|
|
|
|
ENST00000567514.1:n.715+6803C>G
(MKRN2OS)
|
|
|
|
NM_001145392.1:c.1381G>C
(TSEN2)
|
NP_001138864.1:p.Asp461His
|
|
|
NM_001145393.1:c.1303G>C
(TSEN2)
|
NP_001138865.1:p.Asp435His
|
|
|
NM_001145394.1:c.1204G>C
(TSEN2)
|
NP_001138866.1:p.Asp402His
|
|
|
NM_025265.3:c.1381G>C
(TSEN2)
|
NP_079541.1:p.Asp461His
|
|
|
XM_005265495.1:c.1381G>C
(TSEN2)
|
XP_005265552.1:p.Asp461His
|
|
|
XM_005265497.1:c.1303G>C
(TSEN2)
|
XP_005265554.1:p.Asp435His
|
|
|
XM_005265498.1:c.1252G>C
(TSEN2)
|
XP_005265555.1:p.Asp418His
|
|
|
XM_011534138.1:c.1114G>C
(TSEN2)
|
XP_011532440.1:p.Asp372His
|
|
|
XM_011534139.1:c.1108G>C
(TSEN2)
|
XP_011532441.1:p.Asp370His
|
|
|
XR_245158.1:n.1484G>C
(TSEN2)
|
|
|
|
XR_245159.3:n.1484G>C
(TSEN2)
|
|
|
|
XR_427295.2:n.3386G>C
(TSEN2)
|
|
|
|
XR_427296.1:n.1294G>C
(TSEN2)
|
|
|
|
NM_001145393.2:c.1303G>C
(TSEN2)
|
NP_001138865.1:p.Asp435His
|
|
|
NM_001321277.1:c.1381G>C
(TSEN2)
|
NP_001308206.1:p.Asp461His
|
|
|
NM_001321278.1:c.1338+1045G>C
(TSEN2)
|
NP_001308207.1:n.1338+1045G>C
|
|
|
NM_001321279.1:c.1303G>C
(TSEN2)
|
NP_001308208.1:p.Asp435His
|
|
|
NR_135607.1:n.1484G>C
(TSEN2)
|
|
|
|
XM_011534139.3:c.1108G>C
(TSEN2)
|
XP_011532441.1:p.Asp370His
|
|
|
XM_017007292.1:c.1438G>C
(TSEN2)
|
XP_016862781.1:p.Asp480His
|
|
|
XM_017007293.1:c.1438G>C
(TSEN2)
|
XP_016862782.1:p.Asp480His
|
|
|
XM_017007294.1:c.1438G>C
(TSEN2)
|
XP_016862783.1:p.Asp480His
|
|
|
XM_017007295.2:c.1438G>C
(TSEN2)
|
XP_016862784.1:p.Asp480His
|
|
|
XM_017007296.2:c.1381G>C
(TSEN2)
|
XP_016862785.1:p.Asp461His
|
|
|
XM_017007297.1:c.1360G>C
(TSEN2)
|
XP_016862786.1:p.Asp454His
|
|
|
XM_024453785.1:c.1303G>C
(TSEN2)
|
XP_024309553.1:p.Asp435His
|
|
|
XR_001740287.1:n.1825G>C
(TSEN2)
|
|
|
|
XR_001740288.2:n.1825G>C
(TSEN2)
|
|
|
|
XR_001740289.2:n.1768G>C
(TSEN2)
|
|
|
|
XR_001740290.2:n.1382G>C
(TSEN2)
|
|
|
|
XR_001740291.1:n.1690G>C
(TSEN2)
|
|
|
|
XR_001740292.1:n.1788G>C
(TSEN2)
|
|
|
|
XR_001740293.1:n.1788G>C
(TSEN2)
|
|
|
|
XR_001740294.2:n.1423G>C
(TSEN2)
|
|
|
|
XR_001740295.2:n.1345G>C
(TSEN2)
|
|
|
|
XR_001740296.1:n.1635G>C
(TSEN2)
|
|
|
|
XR_001740297.1:n.1953G>C
(TSEN2)
|
|
|
|
XR_001740298.2:n.1270G>C
(TSEN2)
|
|
|
|
XR_001740300.2:n.1588G>C
(TSEN2)
|
|
|
|
XR_001740301.2:n.1588G>C
(TSEN2)
|
|
|
|
XR_001740302.2:n.1551G>C
(TSEN2)
|
|
|
|
XR_001740303.2:n.1398G>C
(TSEN2)
|
|
|
|
XR_001740304.1:n.1706G>C
(TSEN2)
|
|
|
|
XR_002959592.1:n.1559G>C
(TSEN2)
|
|
|
|
XR_002959593.1:n.1516G>C
(TSEN2)
|
|
|
|
XR_002959594.1:n.1556G>C
(TSEN2)
|
|
|
|
XR_002959595.1:n.1896G>C
(TSEN2)
|
|
|
|
XR_427296.2:n.1270G>C
(TSEN2)
|
|
|
|
NM_001321278.2:c.1338+1045G>C
(TSEN2)
|
NP_001308207.1:n.1338+1045G>C
|
|
|
NM_025265.4:c.1381G>C
(TSEN2)
MANE Select
|
NP_079541.1:p.Asp461His
|
|
|
NR_135607.2:n.1436G>C
(TSEN2)
|
|
|
|
NM_001145392.2:c.1381G>C
(TSEN2)
|
NP_001138864.1:p.Asp461His
|
|
|
NM_001145393.3:c.1303G>C
(TSEN2)
|
NP_001138865.1:p.Asp435His
|
|
|
NM_001145394.2:c.1204G>C
(TSEN2)
|
NP_001138866.1:p.Asp402His
|
|
|
NM_001321277.2:c.1381G>C
(TSEN2)
|
NP_001308206.1:p.Asp461His
|
|
|
NM_001321279.2:c.1303G>C
(TSEN2)
|
NP_001308208.1:p.Asp435His
|
|
