|
ENST00000423275.6:c.*1096T>C
(RAF1)
|
ENSP00000401088.1:n.*1096T>C
|
|
|
ENST00000432427.3:c.748T>C
(RAF1)
|
|
|
|
ENST00000460610.2:n.5176T>C
(RAF1)
|
|
|
|
ENST00000471449.2:n.241T>C
(RAF1)
|
|
|
|
ENST00000475353.2:n.3144T>C
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1108T>C
(RAF1)
|
ENSP00000508612.1:n.*1108T>C
|
|
|
ENST00000685348.1:c.*1095-380T>C
(RAF1)
|
ENSP00000510285.1:n.*1095-380T>C
|
|
|
ENST00000685437.1:c.1332T>C
(RAF1)
|
ENSP00000508794.1:p.His444=
|
|
|
ENST00000685653.1:c.1431T>C
(RAF1)
|
ENSP00000509968.1:p.His477=
|
|
|
ENST00000685697.1:n.2166T>C
(RAF1)
|
|
|
|
ENST00000685738.1:c.*395T>C
(RAF1)
|
ENSP00000510156.1:n.*395T>C
|
|
|
ENST00000686409.1:n.4273T>C
(RAF1)
|
|
|
|
ENST00000686455.1:n.3585T>C
(RAF1)
|
|
|
|
ENST00000686762.1:c.1451T>C
(RAF1)
|
ENSP00000509767.1:p.Met484Thr
|
|
|
ENST00000687257.1:n.3458T>C
(RAF1)
|
|
|
|
ENST00000687326.1:c.*2156T>C
(RAF1)
|
ENSP00000509665.1:n.*2156T>C
|
|
|
ENST00000687505.1:n.1549T>C
(RAF1)
|
|
|
|
ENST00000687923.1:c.1320T>C
(RAF1)
|
ENSP00000510255.1:p.His440=
|
|
|
ENST00000688269.1:n.2027T>C
(RAF1)
|
|
|
|
ENST00000688444.1:n.3548T>C
(RAF1)
|
|
|
|
ENST00000688543.1:c.1332T>C
(RAF1)
|
ENSP00000509612.1:p.His444=
|
|
|
ENST00000688625.1:c.*2800T>C
(RAF1)
|
ENSP00000509522.1:n.*2800T>C
|
|
|
ENST00000688803.1:n.2964+489T>C
(RAF1)
|
|
|
|
ENST00000688914.1:n.417T>C
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1108T>C
(RAF1)
|
ENSP00000509756.1:n.*1108T>C
|
|
|
ENST00000689389.1:c.1254T>C
(RAF1)
|
ENSP00000510213.1:p.His418=
|
|
|
ENST00000689418.1:c.*2899T>C
(RAF1)
|
ENSP00000509467.1:n.*2899T>C
|
|
|
ENST00000689540.1:n.3372T>C
(RAF1)
|
|
|
|
ENST00000689876.1:c.1418-380T>C
(RAF1)
|
ENSP00000508535.1:n.1418-380T>C
|
|
|
ENST00000689914.1:c.*365T>C
(RAF1)
|
ENSP00000509847.1:n.*365T>C
|
|
|
ENST00000690397.1:c.1320T>C
(RAF1)
|
ENSP00000508730.1:p.His440=
|
|
|
ENST00000690460.1:c.1419T>C
(RAF1)
|
ENSP00000509106.1:p.His473=
|
|
|
ENST00000690585.1:c.263-533T>C
(RAF1)
|
|
|
|
ENST00000690625.1:n.2467T>C
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1303T>C
(RAF1)
|
ENSP00000510712.1:n.*1303T>C
|
|
|
ENST00000691643.1:n.2057T>C
(RAF1)
|
|
|
|
ENST00000691724.1:c.*388T>C
(RAF1)
|
ENSP00000509255.1:n.*388T>C
|
|
|
ENST00000691779.1:c.*1009T>C
(RAF1)
|
ENSP00000508592.1:n.*1009T>C
|
|
|
ENST00000691888.1:c.310-5T>C
(RAF1)
|
|
|
|
ENST00000691899.1:c.1431T>C
(RAF1)
|
ENSP00000508763.1:p.His477=
|
|
|
ENST00000692069.1:n.3788T>C
(RAF1)
|
|
|
|
ENST00000692093.1:c.1332T>C
(RAF1)
|
ENSP00000509669.1:p.His444=
|
|
|
ENST00000692311.1:n.2255T>C
(RAF1)
|
|
|
|
ENST00000692558.1:n.3587T>C
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1168T>C
(RAF1)
|
ENSP00000509055.1:n.*1168T>C
|
|
|
ENST00000692830.1:c.*1176T>C
(RAF1)
|
ENSP00000509461.1:n.*1176T>C
|
|
|
ENST00000693312.1:c.1206T>C
(RAF1)
|
ENSP00000508686.1:p.His402=
|
|
|
ENST00000693664.1:c.1487+489T>C
(RAF1)
|
ENSP00000509614.1:n.1487+489T>C
|
|
|
ENST00000693705.1:c.*1048-805T>C
(RAF1)
|
ENSP00000510697.1:n.*1048-805T>C
|
|
|
ENST00000251849.9:c.1431T>C
(RAF1)
MANE Select
|
ENSP00000251849.4:p.His477=
|
|
|
ENST00000442415.7:c.1491T>C
(RAF1)
|
ENSP00000401888.2:p.His497=
|
|
|
ENST00000676541.1:c.*3533A>G
(MKRN2)
|
ENSP00000503730.1:n.*3533A>G
|
|
|
ENST00000677142.1:c.*3533A>G
(MKRN2)
|
ENSP00000504455.1:n.*3533A>G
|
|
|
ENST00000677816.1:c.*2088A>G
(MKRN2)
|
ENSP00000502893.1:n.*2088A>G
|
|
|
ENST00000677941.1:n.3596A>G
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1431T>C
(RAF1)
|
ENSP00000251849.4:p.His477=
|
|
|
ENST00000423275.5:c.*1108T>C
(RAF1)
|
ENSP00000401088.1:n.*1108T>C
|
|
|
ENST00000432427.2:c.1068T>C
(RAF1)
|
ENSP00000398591.2:p.His356=
|
|
|
ENST00000442415.6:c.1491T>C
(RAF1)
|
ENSP00000401888.2:p.His497=
|
|
|
ENST00000471449.1:n.120T>C
(RAF1)
|
|
|
|
NM_002880.3:c.1431T>C , LRG_413t1:c.1431T>C
(RAF1)
|
NP_002871.1:p.His477=
|
|
|
XM_005265355.1:c.1431T>C
(RAF1)
|
XP_005265412.1:p.His477=
|
|
|
XM_005265357.1:c.1332T>C
(RAF1)
|
XP_005265414.1:p.His444=
|
|
|
XM_005265358.3:c.1188T>C
(RAF1)
|
XP_005265415.1:p.His396=
|
|
|
XM_005265359.3:c.1089T>C
(RAF1)
|
XP_005265416.1:p.His363=
|
|
|
XM_005265360.1:c.1418-380T>C
(RAF1)
|
XP_005265417.1:n.1418-380T>C
|
|
|
XM_011533974.1:c.1431T>C
(RAF1)
|
XP_011532276.1:p.His477=
|
|
|
XM_011533975.1:c.1188T>C
(RAF1)
|
XP_011532277.1:p.His396=
|
|
|
NM_001354689.1:c.1491T>C
(RAF1)
|
NP_001341618.1:p.His497=
|
|
|
NM_001354690.1:c.1431T>C
(RAF1)
|
NP_001341619.1:p.His477=
|
|
|
NM_001354691.1:c.1188T>C
(RAF1)
|
NP_001341620.1:p.His396=
|
|
|
NM_001354692.1:c.1188T>C
(RAF1)
|
NP_001341621.1:p.His396=
|
|
|
NM_001354693.1:c.1332T>C
(RAF1)
|
NP_001341622.1:p.His444=
|
|
|
NM_001354694.1:c.1248T>C
(RAF1)
|
NP_001341623.1:p.His416=
|
|
|
NM_001354695.1:c.1089T>C
(RAF1)
|
NP_001341624.1:p.His363=
|
|
|
NR_148940.1:n.1959T>C
(RAF1)
|
|
|
|
NR_148941.1:n.1905T>C
(RAF1)
|
|
|
|
NR_148942.1:n.1844T>C
(RAF1)
|
|
|
|
XM_011533974.3:c.1431T>C
(RAF1)
|
XP_011532276.1:p.His477=
|
|
|
XM_017006966.1:c.1332T>C
(RAF1)
|
XP_016862455.1:p.His444=
|
|
|
NM_001354689.3:c.1491T>C
(RAF1)
|
NP_001341618.1:p.His497=
|
|
|
NM_001354690.2:c.1431T>C
(RAF1)
|
NP_001341619.1:p.His477=
|
|
|
NM_001354691.2:c.1188T>C
(RAF1)
|
NP_001341620.1:p.His396=
|
|
|
NM_001354692.2:c.1188T>C
(RAF1)
|
NP_001341621.1:p.His396=
|
|
|
NM_001354693.2:c.1332T>C
(RAF1)
|
NP_001341622.1:p.His444=
|
|
|
NM_001354694.2:c.1248T>C
(RAF1)
|
NP_001341623.1:p.His416=
|
|
|
NM_001354695.2:c.1089T>C
(RAF1)
|
NP_001341624.1:p.His363=
|
|
|
NR_148940.2:n.1875T>C
(RAF1)
|
|
|
|
NR_148941.2:n.1821T>C
(RAF1)
|
|
|
|
NR_148942.2:n.1760T>C
(RAF1)
|
|
|
|
NM_001354690.3:c.1431T>C
(RAF1)
|
NP_001341619.1:p.His477=
|
|
|
NM_001354691.3:c.1188T>C
(RAF1)
|
NP_001341620.1:p.His396=
|
|
|
NM_001354692.3:c.1188T>C
(RAF1)
|
NP_001341621.1:p.His396=
|
|
|
NM_001354693.3:c.1332T>C
(RAF1)
|
NP_001341622.1:p.His444=
|
|
|
NM_001354694.3:c.1248T>C
(RAF1)
|
NP_001341623.1:p.His416=
|
|
|
NM_001354695.3:c.1089T>C
(RAF1)
|
NP_001341624.1:p.His363=
|
|
|
NM_002880.4:c.1431T>C
(RAF1)
MANE Select
|
NP_002871.1:p.His477=
|
|
|
NR_148940.3:n.1875T>C
(RAF1)
|
|
|
|
NR_148941.3:n.1821T>C
(RAF1)
|
|
|
|
NR_148942.3:n.1760T>C
(RAF1)
|
|
|
