|
ENST00000284995.11:c.1376G>C
(TSEN2)
MANE Select
|
ENSP00000284995.6:p.Arg459Thr
|
|
|
ENST00000412698.3:c.1260+1040G>C
(TSEN2)
|
ENSP00000408528.3:n.1260+1040G>C
|
|
|
ENST00000415684.6:c.1298G>C
(TSEN2)
|
ENSP00000416510.1:p.Arg433Thr
|
|
|
ENST00000444864.6:c.1260+1040G>C
(TSEN2)
|
ENSP00000407974.2:n.1260+1040G>C
|
|
|
ENST00000446004.6:c.1338+1040G>C
(TSEN2)
|
ENSP00000406238.2:n.1338+1040G>C
|
|
|
ENST00000455118.6:c.*217G>C
(TSEN2)
|
ENSP00000408744.2:n.*217G>C
|
|
|
ENST00000475595.2:n.4059G>C
(TSEN2)
|
|
|
|
ENST00000679367.1:c.*995G>C
(TSEN2)
|
ENSP00000506510.1:n.*995G>C
|
|
|
ENST00000679420.1:n.1549G>C
(TSEN2)
|
|
|
|
ENST00000679424.1:c.*1219G>C
(TSEN2)
|
ENSP00000505917.1:n.*1219G>C
|
|
|
ENST00000679425.1:c.1376G>C
(TSEN2)
|
ENSP00000505890.1:p.Arg459Thr
|
|
|
ENST00000679492.1:c.1338+1040G>C
(TSEN2)
|
ENSP00000505331.1:n.1338+1040G>C
|
|
|
ENST00000679555.1:c.*1099G>C
(TSEN2)
|
ENSP00000505538.1:n.*1099G>C
|
|
|
ENST00000679670.1:c.1298G>C
(TSEN2)
|
ENSP00000506080.1:p.Arg433Thr
|
|
|
ENST00000679690.1:c.*375G>C
(TSEN2)
|
ENSP00000506383.1:n.*375G>C
|
|
|
ENST00000679693.1:c.*175+1040G>C
(TSEN2)
|
ENSP00000505108.1:n.*175+1040G>C
|
|
|
ENST00000679699.1:c.1376G>C
(TSEN2)
|
ENSP00000505274.1:p.Arg459Thr
|
|
|
ENST00000679756.1:c.1325G>C
(TSEN2)
|
ENSP00000506391.1:p.Arg442Thr
|
|
|
ENST00000679785.1:c.*217G>C
(TSEN2)
|
ENSP00000506473.1:n.*217G>C
|
|
|
ENST00000679835.1:c.*565G>C
(TSEN2)
|
ENSP00000505616.1:n.*565G>C
|
|
|
ENST00000679876.1:c.1209+1040G>C
(TSEN2)
|
ENSP00000504930.1:n.1209+1040G>C
|
|
|
ENST00000679995.1:c.*217G>C
(TSEN2)
|
ENSP00000505221.1:n.*217G>C
|
|
|
ENST00000680126.1:c.*1215G>C
(TSEN2)
|
ENSP00000505345.1:n.*1215G>C
|
|
|
ENST00000680264.1:c.*527+1040G>C
(TSEN2)
|
ENSP00000505273.1:n.*527+1040G>C
|
|
|
ENST00000680275.1:c.1433G>C
(TSEN2)
|
ENSP00000505417.1:p.Arg478Thr
|
|
|
ENST00000680354.1:c.1355G>C
(TSEN2)
|
ENSP00000505106.1:p.Arg452Thr
|
|
|
ENST00000680376.1:c.*565G>C
(TSEN2)
|
ENSP00000506369.1:n.*565G>C
|
|
|
ENST00000680421.1:c.1247G>C
(TSEN2)
|
ENSP00000505530.1:p.Arg416Thr
|
|
|
ENST00000680449.1:c.*518G>C
(TSEN2)
|
ENSP00000505709.1:n.*518G>C
|
|
|
ENST00000680458.1:c.*191G>C
(TSEN2)
|
ENSP00000505979.1:n.*191G>C
|
|
|
ENST00000680555.1:c.*217G>C
(TSEN2)
|
ENSP00000505160.1:n.*217G>C
|
|
|
ENST00000680598.1:c.1325G>C
(TSEN2)
|
ENSP00000506297.1:p.Arg442Thr
|
|
|
ENST00000680765.1:c.*217G>C
(TSEN2)
|
ENSP00000505351.1:n.*217G>C
|
|
|
ENST00000680817.1:c.1247G>C
(TSEN2)
|
ENSP00000506221.1:p.Arg416Thr
|
|
|
ENST00000680857.1:c.1338+1040G>C
(TSEN2)
|
ENSP00000506578.1:n.1338+1040G>C
|
|
|
ENST00000680873.1:c.*528G>C
(TSEN2)
|
ENSP00000505233.1:n.*528G>C
|
|
|
ENST00000680923.1:c.*565G>C
(TSEN2)
|
ENSP00000505344.1:n.*565G>C
|
|
|
ENST00000680943.1:c.1325G>C
(TSEN2)
|
ENSP00000505442.1:p.Arg442Thr
|
|
|
ENST00000680986.1:c.1376G>C
(TSEN2)
|
ENSP00000505799.1:p.Arg459Thr
|
|
|
ENST00000681042.1:c.1100-6462G>C
(TSEN2)
|
ENSP00000505622.1:n.1100-6462G>C
|
|
|
ENST00000681073.1:c.*217G>C
(TSEN2)
|
ENSP00000506576.1:n.*217G>C
|
|
|
ENST00000681140.1:c.1376G>C
(TSEN2)
|
ENSP00000505099.1:p.Arg459Thr
|
|
|
ENST00000681227.1:c.*248G>C
(TSEN2)
|
ENSP00000505240.1:n.*248G>C
|
|
|
ENST00000681268.1:c.*1520G>C
(TSEN2)
|
ENSP00000505385.1:n.*1520G>C
|
|
|
ENST00000681343.1:c.*995G>C
(TSEN2)
|
ENSP00000506265.1:n.*995G>C
|
|
|
ENST00000681433.1:c.*217G>C
(TSEN2)
|
ENSP00000505729.1:n.*217G>C
|
|
|
ENST00000681471.1:c.1298G>C
(TSEN2)
|
ENSP00000505105.1:p.Arg433Thr
|
|
|
ENST00000681482.1:c.1376G>C
(TSEN2)
|
ENSP00000505436.1:p.Arg459Thr
|
|
|
ENST00000681676.1:c.1298G>C
(TSEN2)
|
ENSP00000506163.1:p.Arg433Thr
|
|
|
ENST00000681713.1:c.*995G>C
(TSEN2)
|
ENSP00000506046.1:n.*995G>C
|
|
|
ENST00000284995.10:c.1376G>C
(TSEN2)
|
ENSP00000284995.6:p.Arg459Thr
|
|
|
ENST00000402228.7:c.1376G>C
(TSEN2)
|
ENSP00000385976.3:p.Arg459Thr
|
|
|
ENST00000412698.2:c.93+1040G>C
(TSEN2)
|
ENSP00000408528.2:n.93+1040G>C
|
|
|
ENST00000415684.5:c.1298G>C
(TSEN2)
|
ENSP00000416510.1:p.Arg433Thr
|
|
|
ENST00000454502.6:c.1199G>C
(TSEN2)
|
ENSP00000392029.2:p.Arg400Thr
|
|
|
ENST00000455118.5:c.223G>C
(TSEN2)
|
|
|
|
ENST00000473755.5:n.3381G>C
(TSEN2)
|
|
|
|
ENST00000475595.1:n.222G>C
(TSEN2)
|
|
|
|
ENST00000567514.1:n.715+6808C>G
(MKRN2OS)
|
|
|
|
NM_001145392.1:c.1376G>C
(TSEN2)
|
NP_001138864.1:p.Arg459Thr
|
|
|
NM_001145393.1:c.1298G>C
(TSEN2)
|
NP_001138865.1:p.Arg433Thr
|
|
|
NM_001145394.1:c.1199G>C
(TSEN2)
|
NP_001138866.1:p.Arg400Thr
|
|
|
NM_025265.3:c.1376G>C
(TSEN2)
|
NP_079541.1:p.Arg459Thr
|
|
|
XM_005265495.1:c.1376G>C
(TSEN2)
|
XP_005265552.1:p.Arg459Thr
|
|
|
XM_005265497.1:c.1298G>C
(TSEN2)
|
XP_005265554.1:p.Arg433Thr
|
|
|
XM_005265498.1:c.1247G>C
(TSEN2)
|
XP_005265555.1:p.Arg416Thr
|
|
|
XM_011534138.1:c.1109G>C
(TSEN2)
|
XP_011532440.1:p.Arg370Thr
|
|
|
XM_011534139.1:c.1103G>C
(TSEN2)
|
XP_011532441.1:p.Arg368Thr
|
|
|
XR_245158.1:n.1479G>C
(TSEN2)
|
|
|
|
XR_245159.3:n.1479G>C
(TSEN2)
|
|
|
|
XR_427295.2:n.3381G>C
(TSEN2)
|
|
|
|
XR_427296.1:n.1289G>C
(TSEN2)
|
|
|
|
NM_001145393.2:c.1298G>C
(TSEN2)
|
NP_001138865.1:p.Arg433Thr
|
|
|
NM_001321277.1:c.1376G>C
(TSEN2)
|
NP_001308206.1:p.Arg459Thr
|
|
|
NM_001321278.1:c.1338+1040G>C
(TSEN2)
|
NP_001308207.1:n.1338+1040G>C
|
|
|
NM_001321279.1:c.1298G>C
(TSEN2)
|
NP_001308208.1:p.Arg433Thr
|
|
|
NR_135607.1:n.1479G>C
(TSEN2)
|
|
|
|
XM_011534139.3:c.1103G>C
(TSEN2)
|
XP_011532441.1:p.Arg368Thr
|
|
|
XM_017007292.1:c.1433G>C
(TSEN2)
|
XP_016862781.1:p.Arg478Thr
|
|
|
XM_017007293.1:c.1433G>C
(TSEN2)
|
XP_016862782.1:p.Arg478Thr
|
|
|
XM_017007294.1:c.1433G>C
(TSEN2)
|
XP_016862783.1:p.Arg478Thr
|
|
|
XM_017007295.2:c.1433G>C
(TSEN2)
|
XP_016862784.1:p.Arg478Thr
|
|
|
XM_017007296.2:c.1376G>C
(TSEN2)
|
XP_016862785.1:p.Arg459Thr
|
|
|
XM_017007297.1:c.1355G>C
(TSEN2)
|
XP_016862786.1:p.Arg452Thr
|
|
|
XM_024453785.1:c.1298G>C
(TSEN2)
|
XP_024309553.1:p.Arg433Thr
|
|
|
XR_001740287.1:n.1820G>C
(TSEN2)
|
|
|
|
XR_001740288.2:n.1820G>C
(TSEN2)
|
|
|
|
XR_001740289.2:n.1763G>C
(TSEN2)
|
|
|
|
XR_001740290.2:n.1377G>C
(TSEN2)
|
|
|
|
XR_001740291.1:n.1685G>C
(TSEN2)
|
|
|
|
XR_001740292.1:n.1783G>C
(TSEN2)
|
|
|
|
XR_001740293.1:n.1783G>C
(TSEN2)
|
|
|
|
XR_001740294.2:n.1418G>C
(TSEN2)
|
|
|
|
XR_001740295.2:n.1340G>C
(TSEN2)
|
|
|
|
XR_001740296.1:n.1630G>C
(TSEN2)
|
|
|
|
XR_001740297.1:n.1948G>C
(TSEN2)
|
|
|
|
XR_001740298.2:n.1265G>C
(TSEN2)
|
|
|
|
XR_001740300.2:n.1583G>C
(TSEN2)
|
|
|
|
XR_001740301.2:n.1583G>C
(TSEN2)
|
|
|
|
XR_001740302.2:n.1546G>C
(TSEN2)
|
|
|
|
XR_001740303.2:n.1393G>C
(TSEN2)
|
|
|
|
XR_001740304.1:n.1701G>C
(TSEN2)
|
|
|
|
XR_002959592.1:n.1554G>C
(TSEN2)
|
|
|
|
XR_002959593.1:n.1511G>C
(TSEN2)
|
|
|
|
XR_002959594.1:n.1551G>C
(TSEN2)
|
|
|
|
XR_002959595.1:n.1891G>C
(TSEN2)
|
|
|
|
XR_427296.2:n.1265G>C
(TSEN2)
|
|
|
|
NM_001321278.2:c.1338+1040G>C
(TSEN2)
|
NP_001308207.1:n.1338+1040G>C
|
|
|
NM_025265.4:c.1376G>C
(TSEN2)
MANE Select
|
NP_079541.1:p.Arg459Thr
|
|
|
NR_135607.2:n.1431G>C
(TSEN2)
|
|
|
|
NM_001145392.2:c.1376G>C
(TSEN2)
|
NP_001138864.1:p.Arg459Thr
|
|
|
NM_001145393.3:c.1298G>C
(TSEN2)
|
NP_001138865.1:p.Arg433Thr
|
|
|
NM_001145394.2:c.1199G>C
(TSEN2)
|
NP_001138866.1:p.Arg400Thr
|
|
|
NM_001321277.2:c.1376G>C
(TSEN2)
|
NP_001308206.1:p.Arg459Thr
|
|
|
NM_001321279.2:c.1298G>C
(TSEN2)
|
NP_001308208.1:p.Arg433Thr
|
|
