|
ENST00000682236.1:n.2953G>C
|
|
|
|
ENST00000682536.1:c.4094G>C
|
ENSP00000507956.1:p.Ser1365Thr
|
|
|
ENST00000687014.1:n.4987G>C
|
|
|
|
ENST00000689167.1:n.2378G>C
|
|
|
|
ENST00000693430.1:n.6240G>C
|
|
|
|
ENST00000402198.7:c.3998G>C
MANE Select
|
ENSP00000385852.2:p.Ser1333Thr
|
|
|
ENST00000663774.1:c.*4144G>C
|
ENSP00000499452.1:n.*4144G>C
|
|
|
ENST00000665872.1:c.*4067G>C
|
ENSP00000499600.1:n.*4067G>C
|
|
|
ENST00000666307.1:c.*4372G>C
|
ENSP00000499402.1:n.*4372G>C
|
|
|
ENST00000670063.1:c.*4103G>C
|
ENSP00000499725.1:n.*4103G>C
|
|
|
ENST00000302463.10:c.3704G>C
|
ENSP00000302028.6:p.Ser1235Thr
|
|
|
ENST00000399686.6:c.2722+604G>C
|
|
|
|
ENST00000402198.5:c.3998G>C
|
ENSP00000385852.1:p.Ser1333Thr
|
|
|
ENST00000406341.5:c.3998G>C
|
ENSP00000383939.1:p.Ser1333Thr
|
|
|
ENST00000407969.5:c.4055G>C
|
ENSP00000384114.1:p.Ser1352Thr
|
|
|
ENST00000413704.5:c.3034G>C
|
|
|
|
ENST00000466242.5:n.3339G>C
|
|
|
|
ENST00000493918.5:n.4162G>C
|
|
|
|
NM_001080517.2:c.3998G>C
|
NP_001073986.1:p.Ser1333Thr
|
|
|
NM_001292043.1:c.3704G>C
|
NP_001278972.1:p.Ser1235Thr
|
|
|
XM_005265301.1:c.4055G>C
|
XP_005265358.1:p.Ser1352Thr
|
|
|
XM_005265303.1:c.3998G>C
|
XP_005265360.1:p.Ser1333Thr
|
|
|
XM_011533920.1:c.4172G>C
|
XP_011532222.1:p.Ser1391Thr
|
|
|
XM_011533921.1:c.4172G>C
|
XP_011532223.1:p.Ser1391Thr
|
|
|
XM_011533922.1:c.4151G>C
|
XP_011532224.1:p.Ser1384Thr
|
|
|
XM_011533923.1:c.4151G>C
|
XP_011532225.1:p.Ser1384Thr
|
|
|
XM_011533924.1:c.4151G>C
|
XP_011532226.1:p.Ser1384Thr
|
|
|
XM_011533925.1:c.4133G>C
|
XP_011532227.1:p.Ser1378Thr
|
|
|
XM_011533926.1:c.4115G>C
|
XP_011532228.1:p.Ser1372Thr
|
|
|
XM_011533927.1:c.4115G>C
|
XP_011532229.1:p.Ser1372Thr
|
|
|
XM_011533928.1:c.4094G>C
|
XP_011532230.1:p.Ser1365Thr
|
|
|
XM_011533929.1:c.4076G>C
|
XP_011532231.1:p.Ser1359Thr
|
|
|
XM_011533930.1:c.4037G>C
|
XP_011532232.1:p.Ser1346Thr
|
|
|
XM_011533931.1:c.3761G>C
|
XP_011532233.1:p.Ser1254Thr
|
|
|
XM_011533932.1:c.3722G>C
|
XP_011532234.1:p.Ser1241Thr
|
|
|
XM_011533933.1:c.3722G>C
|
XP_011532235.1:p.Ser1241Thr
|
|
|
NM_001349451.1:c.3704G>C
|
NP_001336380.1:p.Ser1235Thr
|
|
|
XM_011533921.2:c.4172G>C
|
XP_011532223.1:p.Ser1391Thr
|
|
|
XM_017006767.1:c.4172G>C
|
XP_016862256.1:p.Ser1391Thr
|
|
|
XM_017006768.2:c.4151G>C
|
XP_016862257.1:p.Ser1384Thr
|
|
|
XM_017006770.1:c.4115G>C
|
XP_016862259.1:p.Ser1372Thr
|
|
|
XM_017006771.1:c.4112G>C
|
XP_016862260.1:p.Ser1371Thr
|
|
|
XM_017006772.1:c.4076G>C
|
XP_016862261.1:p.Ser1359Thr
|
|
|
XM_017006773.1:c.4076G>C
|
XP_016862262.1:p.Ser1359Thr
|
|
|
XM_017006774.1:c.4055G>C
|
XP_016862263.1:p.Ser1352Thr
|
|
|
XM_017006775.1:c.4019G>C
|
XP_016862264.1:p.Ser1340Thr
|
|
|
XM_017006776.1:c.3761G>C
|
XP_016862265.1:p.Ser1254Thr
|
|
|
XM_017006777.1:c.3761G>C
|
XP_016862266.1:p.Ser1254Thr
|
|
|
XM_017006778.1:c.3761G>C
|
XP_016862267.1:p.Ser1254Thr
|
|
|
XM_017006779.1:c.3722G>C
|
XP_016862268.1:p.Ser1241Thr
|
|
|
XM_017006780.1:c.3722G>C
|
XP_016862269.1:p.Ser1241Thr
|
|
|
XM_017006783.1:c.3494G>C
|
XP_016862272.1:p.Ser1165Thr
|
|
|
XM_024453620.1:c.4133G>C
|
XP_024309388.1:p.Ser1378Thr
|
|
|
XM_024453621.1:c.3809G>C
|
XP_024309389.1:p.Ser1270Thr
|
|
|
XR_001740195.2:n.8381G>C
|
|
|
|
NM_001080517.3:c.3998G>C
MANE Select
|
NP_001073986.1:p.Ser1333Thr
|
|
|
NM_001292043.2:c.3704G>C
|
NP_001278972.1:p.Ser1235Thr
|
|
|
NM_001349451.2:c.3704G>C
|
NP_001336380.1:p.Ser1235Thr
|
|
