ENST00000682236.1:n.2740T>A
|
|
|
ENST00000682536.1:c.3881T>A
|
ENSP00000507956.1:p.Phe1294Tyr
|
|
ENST00000687014.1:n.4774T>A
|
|
|
ENST00000689167.1:n.2165T>A
|
|
|
ENST00000691925.1:n.6582T>A
|
|
|
ENST00000693430.1:n.6027T>A
|
|
|
ENST00000402198.7:c.3785T>A
MANE Select
|
ENSP00000385852.2:p.Phe1262Tyr
|
|
ENST00000663774.1:c.*3931T>A
|
ENSP00000499452.1:n.*3931T>A
|
|
ENST00000665872.1:c.*3854T>A
|
ENSP00000499600.1:n.*3854T>A
|
|
ENST00000666307.1:c.*4159T>A
|
ENSP00000499402.1:n.*4159T>A
|
|
ENST00000670063.1:c.*3890T>A
|
ENSP00000499725.1:n.*3890T>A
|
|
ENST00000302463.10:c.3491T>A
|
ENSP00000302028.6:p.Phe1164Tyr
|
|
ENST00000399686.6:c.2722+391T>A
|
|
|
ENST00000402198.5:c.3785T>A
|
ENSP00000385852.1:p.Phe1262Tyr
|
|
ENST00000406341.5:c.3785T>A
|
ENSP00000383939.1:p.Phe1262Tyr
|
|
ENST00000407969.5:c.3842T>A
|
ENSP00000384114.1:p.Phe1281Tyr
|
|
ENST00000413704.5:c.2821T>A
|
|
|
ENST00000459941.1:n.916T>A
|
|
|
ENST00000466242.5:n.3126T>A
|
|
|
ENST00000466826.1:n.172T>A
|
|
|
ENST00000493918.5:n.3949T>A
|
|
|
NM_001080517.2:c.3785T>A
|
NP_001073986.1:p.Phe1262Tyr
|
|
NM_001292043.1:c.3491T>A
|
NP_001278972.1:p.Phe1164Tyr
|
|
XM_005265301.1:c.3842T>A
|
XP_005265358.1:p.Phe1281Tyr
|
|
XM_005265303.1:c.3785T>A
|
XP_005265360.1:p.Phe1262Tyr
|
|
XM_011533920.1:c.3959T>A
|
XP_011532222.1:p.Phe1320Tyr
|
|
XM_011533921.1:c.3959T>A
|
XP_011532223.1:p.Phe1320Tyr
|
|
XM_011533922.1:c.3938T>A
|
XP_011532224.1:p.Phe1313Tyr
|
|
XM_011533923.1:c.3938T>A
|
XP_011532225.1:p.Phe1313Tyr
|
|
XM_011533924.1:c.3938T>A
|
XP_011532226.1:p.Phe1313Tyr
|
|
XM_011533925.1:c.3920T>A
|
XP_011532227.1:p.Phe1307Tyr
|
|
XM_011533926.1:c.3902T>A
|
XP_011532228.1:p.Phe1301Tyr
|
|
XM_011533927.1:c.3902T>A
|
XP_011532229.1:p.Phe1301Tyr
|
|
XM_011533928.1:c.3881T>A
|
XP_011532230.1:p.Phe1294Tyr
|
|
XM_011533929.1:c.3863T>A
|
XP_011532231.1:p.Phe1288Tyr
|
|
XM_011533930.1:c.3824T>A
|
XP_011532232.1:p.Phe1275Tyr
|
|
XM_011533931.1:c.3548T>A
|
XP_011532233.1:p.Phe1183Tyr
|
|
XM_011533932.1:c.3509T>A
|
XP_011532234.1:p.Phe1170Tyr
|
|
XM_011533933.1:c.3509T>A
|
XP_011532235.1:p.Phe1170Tyr
|
|
NM_001349451.1:c.3491T>A
|
NP_001336380.1:p.Phe1164Tyr
|
|
XM_011533921.2:c.3959T>A
|
XP_011532223.1:p.Phe1320Tyr
|
|
XM_017006767.1:c.3959T>A
|
XP_016862256.1:p.Phe1320Tyr
|
|
XM_017006768.2:c.3938T>A
|
XP_016862257.1:p.Phe1313Tyr
|
|
XM_017006770.1:c.3902T>A
|
XP_016862259.1:p.Phe1301Tyr
|
|
XM_017006771.1:c.3899T>A
|
XP_016862260.1:p.Phe1300Tyr
|
|
XM_017006772.1:c.3863T>A
|
XP_016862261.1:p.Phe1288Tyr
|
|
XM_017006773.1:c.3863T>A
|
XP_016862262.1:p.Phe1288Tyr
|
|
XM_017006774.1:c.3842T>A
|
XP_016862263.1:p.Phe1281Tyr
|
|
XM_017006775.1:c.3806T>A
|
XP_016862264.1:p.Phe1269Tyr
|
|
XM_017006776.1:c.3548T>A
|
XP_016862265.1:p.Phe1183Tyr
|
|
XM_017006777.1:c.3548T>A
|
XP_016862266.1:p.Phe1183Tyr
|
|
XM_017006778.1:c.3548T>A
|
XP_016862267.1:p.Phe1183Tyr
|
|
XM_017006779.1:c.3509T>A
|
XP_016862268.1:p.Phe1170Tyr
|
|
XM_017006780.1:c.3509T>A
|
XP_016862269.1:p.Phe1170Tyr
|
|
XM_017006783.1:c.3281T>A
|
XP_016862272.1:p.Phe1094Tyr
|
|
XM_024453620.1:c.3920T>A
|
XP_024309388.1:p.Phe1307Tyr
|
|
XM_024453621.1:c.3596T>A
|
XP_024309389.1:p.Phe1199Tyr
|
|
XR_001740195.2:n.8168T>A
|
|
|
NM_001080517.3:c.3785T>A
MANE Select
|
NP_001073986.1:p.Phe1262Tyr
|
|
NM_001292043.2:c.3491T>A
|
NP_001278972.1:p.Phe1164Tyr
|
|
NM_001349451.2:c.3491T>A
|
NP_001336380.1:p.Phe1164Tyr
|
|