|
ENST00000682236.1:n.2900G>C
|
|
|
|
ENST00000682536.1:c.4041G>C
|
ENSP00000507956.1:p.Thr1347=
|
|
|
ENST00000687014.1:n.4934G>C
|
|
|
|
ENST00000689167.1:n.2325G>C
|
|
|
|
ENST00000693430.1:n.6187G>C
|
|
|
|
ENST00000402198.7:c.3945G>C
MANE Select
|
ENSP00000385852.2:p.Thr1315=
|
|
|
ENST00000663774.1:c.*4091G>C
|
ENSP00000499452.1:n.*4091G>C
|
|
|
ENST00000665872.1:c.*4014G>C
|
ENSP00000499600.1:n.*4014G>C
|
|
|
ENST00000666307.1:c.*4319G>C
|
ENSP00000499402.1:n.*4319G>C
|
|
|
ENST00000670063.1:c.*4050G>C
|
ENSP00000499725.1:n.*4050G>C
|
|
|
ENST00000302463.10:c.3651G>C
|
ENSP00000302028.6:p.Thr1217=
|
|
|
ENST00000399686.6:c.2722+551G>C
|
|
|
|
ENST00000402198.5:c.3945G>C
|
ENSP00000385852.1:p.Thr1315=
|
|
|
ENST00000406341.5:c.3945G>C
|
ENSP00000383939.1:p.Thr1315=
|
|
|
ENST00000407969.5:c.4002G>C
|
ENSP00000384114.1:p.Thr1334=
|
|
|
ENST00000413704.5:c.2981G>C
|
|
|
|
ENST00000466242.5:n.3286G>C
|
|
|
|
ENST00000493918.5:n.4109G>C
|
|
|
|
NM_001080517.2:c.3945G>C
|
NP_001073986.1:p.Thr1315=
|
|
|
NM_001292043.1:c.3651G>C
|
NP_001278972.1:p.Thr1217=
|
|
|
XM_005265301.1:c.4002G>C
|
XP_005265358.1:p.Thr1334=
|
|
|
XM_005265303.1:c.3945G>C
|
XP_005265360.1:p.Thr1315=
|
|
|
XM_011533920.1:c.4119G>C
|
XP_011532222.1:p.Thr1373=
|
|
|
XM_011533921.1:c.4119G>C
|
XP_011532223.1:p.Thr1373=
|
|
|
XM_011533922.1:c.4098G>C
|
XP_011532224.1:p.Thr1366=
|
|
|
XM_011533923.1:c.4098G>C
|
XP_011532225.1:p.Thr1366=
|
|
|
XM_011533924.1:c.4098G>C
|
XP_011532226.1:p.Thr1366=
|
|
|
XM_011533925.1:c.4080G>C
|
XP_011532227.1:p.Thr1360=
|
|
|
XM_011533926.1:c.4062G>C
|
XP_011532228.1:p.Thr1354=
|
|
|
XM_011533927.1:c.4062G>C
|
XP_011532229.1:p.Thr1354=
|
|
|
XM_011533928.1:c.4041G>C
|
XP_011532230.1:p.Thr1347=
|
|
|
XM_011533929.1:c.4023G>C
|
XP_011532231.1:p.Thr1341=
|
|
|
XM_011533930.1:c.3984G>C
|
XP_011532232.1:p.Thr1328=
|
|
|
XM_011533931.1:c.3708G>C
|
XP_011532233.1:p.Thr1236=
|
|
|
XM_011533932.1:c.3669G>C
|
XP_011532234.1:p.Thr1223=
|
|
|
XM_011533933.1:c.3669G>C
|
XP_011532235.1:p.Thr1223=
|
|
|
NM_001349451.1:c.3651G>C
|
NP_001336380.1:p.Thr1217=
|
|
|
XM_011533921.2:c.4119G>C
|
XP_011532223.1:p.Thr1373=
|
|
|
XM_017006767.1:c.4119G>C
|
XP_016862256.1:p.Thr1373=
|
|
|
XM_017006768.2:c.4098G>C
|
XP_016862257.1:p.Thr1366=
|
|
|
XM_017006770.1:c.4062G>C
|
XP_016862259.1:p.Thr1354=
|
|
|
XM_017006771.1:c.4059G>C
|
XP_016862260.1:p.Thr1353=
|
|
|
XM_017006772.1:c.4023G>C
|
XP_016862261.1:p.Thr1341=
|
|
|
XM_017006773.1:c.4023G>C
|
XP_016862262.1:p.Thr1341=
|
|
|
XM_017006774.1:c.4002G>C
|
XP_016862263.1:p.Thr1334=
|
|
|
XM_017006775.1:c.3966G>C
|
XP_016862264.1:p.Thr1322=
|
|
|
XM_017006776.1:c.3708G>C
|
XP_016862265.1:p.Thr1236=
|
|
|
XM_017006777.1:c.3708G>C
|
XP_016862266.1:p.Thr1236=
|
|
|
XM_017006778.1:c.3708G>C
|
XP_016862267.1:p.Thr1236=
|
|
|
XM_017006779.1:c.3669G>C
|
XP_016862268.1:p.Thr1223=
|
|
|
XM_017006780.1:c.3669G>C
|
XP_016862269.1:p.Thr1223=
|
|
|
XM_017006783.1:c.3441G>C
|
XP_016862272.1:p.Thr1147=
|
|
|
XM_024453620.1:c.4080G>C
|
XP_024309388.1:p.Thr1360=
|
|
|
XM_024453621.1:c.3756G>C
|
XP_024309389.1:p.Thr1252=
|
|
|
XR_001740195.2:n.8328G>C
|
|
|
|
NM_001080517.3:c.3945G>C
MANE Select
|
NP_001073986.1:p.Thr1315=
|
|
|
NM_001292043.2:c.3651G>C
|
NP_001278972.1:p.Thr1217=
|
|
|
NM_001349451.2:c.3651G>C
|
NP_001336380.1:p.Thr1217=
|
|
