|
ENST00000423275.6:c.*1571G>A
(RAF1)
|
ENSP00000401088.1:n.*1571G>A
|
|
|
ENST00000432427.3:c.1223G>A
(RAF1)
|
|
|
|
ENST00000460610.2:n.6218G>A
(RAF1)
|
|
|
|
ENST00000471449.2:n.716G>A
(RAF1)
|
|
|
|
ENST00000475353.2:n.4186G>A
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1583G>A
(RAF1)
|
ENSP00000508612.1:n.*1583G>A
|
|
|
ENST00000685348.1:c.*1617G>A
(RAF1)
|
ENSP00000510285.1:n.*1617G>A
|
|
|
ENST00000685437.1:c.1807G>A
(RAF1)
|
ENSP00000508794.1:p.Ala603Thr
|
|
|
ENST00000685653.1:c.1906G>A
(RAF1)
|
ENSP00000509968.1:p.Ala636Thr
|
|
|
ENST00000685697.1:n.2641G>A
(RAF1)
|
|
|
|
ENST00000685738.1:c.*870G>A
(RAF1)
|
ENSP00000510156.1:n.*870G>A
|
|
|
ENST00000686409.1:n.5315G>A
(RAF1)
|
|
|
|
ENST00000686455.1:n.4627G>A
(RAF1)
|
|
|
|
ENST00000686762.1:c.*465G>A
(RAF1)
|
ENSP00000509767.1:n.*465G>A
|
|
|
ENST00000687257.1:n.4360G>A
(RAF1)
|
|
|
|
ENST00000687326.1:c.*3198G>A
(RAF1)
|
ENSP00000509665.1:n.*3198G>A
|
|
|
ENST00000687505.1:n.2024G>A
(RAF1)
|
|
|
|
ENST00000687923.1:c.1795G>A
(RAF1)
|
ENSP00000510255.1:p.Ala599Thr
|
|
|
ENST00000688269.1:n.2502G>A
(RAF1)
|
|
|
|
ENST00000688444.1:n.4023G>A
(RAF1)
|
|
|
|
ENST00000688543.1:c.1807G>A
(RAF1)
|
ENSP00000509612.1:p.Ala603Thr
|
|
|
ENST00000688625.1:c.*3275G>A
(RAF1)
|
ENSP00000509522.1:n.*3275G>A
|
|
|
ENST00000688803.1:n.3334G>A
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1583G>A
(RAF1)
|
ENSP00000509756.1:n.*1583G>A
|
|
|
ENST00000689389.1:c.1729G>A
(RAF1)
|
ENSP00000510213.1:p.Ala577Thr
|
|
|
ENST00000689418.1:c.*3801G>A
(RAF1)
|
ENSP00000509467.1:n.*3801G>A
|
|
|
ENST00000689540.1:n.4274G>A
(RAF1)
|
|
|
|
ENST00000689876.1:c.*455G>A
(RAF1)
|
ENSP00000508535.1:n.*455G>A
|
|
|
ENST00000689914.1:c.*840G>A
(RAF1)
|
ENSP00000509847.1:n.*840G>A
|
|
|
ENST00000690397.1:c.1795G>A
(RAF1)
|
ENSP00000508730.1:p.Ala599Thr
|
|
|
ENST00000690460.1:c.1894G>A
(RAF1)
|
ENSP00000509106.1:p.Ala632Thr
|
|
|
ENST00000690585.1:c.632G>A
(RAF1)
|
|
|
|
ENST00000690625.1:n.2942G>A
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1778G>A
(RAF1)
|
ENSP00000510712.1:n.*1778G>A
|
|
|
ENST00000691643.1:n.2959G>A
(RAF1)
|
|
|
|
ENST00000691724.1:c.*863G>A
(RAF1)
|
ENSP00000509255.1:n.*863G>A
|
|
|
ENST00000691779.1:c.*1484G>A
(RAF1)
|
ENSP00000508592.1:n.*1484G>A
|
|
|
ENST00000691888.1:c.780G>A
(RAF1)
|
|
|
|
ENST00000691899.1:c.1906G>A
(RAF1)
|
ENSP00000508763.1:p.Ala636Thr
|
|
|
ENST00000692069.1:n.4830G>A
(RAF1)
|
|
|
|
ENST00000692093.1:c.1807G>A
(RAF1)
|
ENSP00000509669.1:p.Ala603Thr
|
|
|
ENST00000692311.1:n.2730G>A
(RAF1)
|
|
|
|
ENST00000692558.1:n.4489G>A
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1643G>A
(RAF1)
|
ENSP00000509055.1:n.*1643G>A
|
|
|
ENST00000692830.1:c.*1651G>A
(RAF1)
|
ENSP00000509461.1:n.*1651G>A
|
|
|
ENST00000693312.1:c.1681G>A
(RAF1)
|
ENSP00000508686.1:p.Ala561Thr
|
|
|
ENST00000693664.1:c.*357G>A
(RAF1)
|
ENSP00000509614.1:n.*357G>A
|
|
|
ENST00000693705.1:c.*1285G>A
(RAF1)
|
ENSP00000510697.1:n.*1285G>A
|
|
|
ENST00000251849.9:c.1906G>A
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Ala636Thr
|
|
|
ENST00000442415.7:c.1966G>A
(RAF1)
|
ENSP00000401888.2:p.Ala656Thr
|
|
|
ENST00000676541.1:c.*2302C>T
(MKRN2)
|
ENSP00000503730.1:n.*2302C>T
|
|
|
ENST00000677142.1:c.*2302C>T
(MKRN2)
|
ENSP00000504455.1:n.*2302C>T
|
|
|
ENST00000677816.1:c.*857C>T
(MKRN2)
|
ENSP00000502893.1:n.*857C>T
|
|
|
ENST00000677941.1:n.2365C>T
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1906G>A
(RAF1)
|
ENSP00000251849.4:p.Ala636Thr
|
|
|
ENST00000423275.5:c.*1583G>A
(RAF1)
|
ENSP00000401088.1:n.*1583G>A
|
|
|
ENST00000432427.2:c.1543G>A
(RAF1)
|
ENSP00000398591.2:p.Ala515Thr
|
|
|
ENST00000442415.6:c.1966G>A
(RAF1)
|
ENSP00000401888.2:p.Ala656Thr
|
|
|
ENST00000471449.1:n.595G>A
(RAF1)
|
|
|
|
NM_002880.3:c.1906G>A , LRG_413t1:c.1906G>A
(RAF1)
|
NP_002871.1:p.Ala636Thr
|
|
|
XM_005265355.1:c.1906G>A
(RAF1)
|
XP_005265412.1:p.Ala636Thr
|
|
|
XM_005265357.1:c.1807G>A
(RAF1)
|
XP_005265414.1:p.Ala603Thr
|
|
|
XM_005265358.3:c.1663G>A
(RAF1)
|
XP_005265415.1:p.Ala555Thr
|
|
|
XM_005265359.3:c.1564G>A
(RAF1)
|
XP_005265416.1:p.Ala522Thr
|
|
|
XM_011533974.1:c.1906G>A
(RAF1)
|
XP_011532276.1:p.Ala636Thr
|
|
|
XM_011533975.1:c.1663G>A
(RAF1)
|
XP_011532277.1:p.Ala555Thr
|
|
|
NM_001354689.1:c.1966G>A
(RAF1)
|
NP_001341618.1:p.Ala656Thr
|
|
|
NM_001354690.1:c.1906G>A
(RAF1)
|
NP_001341619.1:p.Ala636Thr
|
|
|
NM_001354691.1:c.1663G>A
(RAF1)
|
NP_001341620.1:p.Ala555Thr
|
|
|
NM_001354692.1:c.1663G>A
(RAF1)
|
NP_001341621.1:p.Ala555Thr
|
|
|
NM_001354693.1:c.1807G>A
(RAF1)
|
NP_001341622.1:p.Ala603Thr
|
|
|
NM_001354694.1:c.1723G>A
(RAF1)
|
NP_001341623.1:p.Ala575Thr
|
|
|
NM_001354695.1:c.1564G>A
(RAF1)
|
NP_001341624.1:p.Ala522Thr
|
|
|
NR_148940.1:n.2434G>A
(RAF1)
|
|
|
|
NR_148941.1:n.2380G>A
(RAF1)
|
|
|
|
NR_148942.1:n.2319G>A
(RAF1)
|
|
|
|
XM_011533974.3:c.1906G>A
(RAF1)
|
XP_011532276.1:p.Ala636Thr
|
|
|
XM_017006966.1:c.1807G>A
(RAF1)
|
XP_016862455.1:p.Ala603Thr
|
|
|
NM_001354689.3:c.1966G>A
(RAF1)
|
NP_001341618.1:p.Ala656Thr
|
|
|
NM_001354690.2:c.1906G>A
(RAF1)
|
NP_001341619.1:p.Ala636Thr
|
|
|
NM_001354691.2:c.1663G>A
(RAF1)
|
NP_001341620.1:p.Ala555Thr
|
|
|
NM_001354692.2:c.1663G>A
(RAF1)
|
NP_001341621.1:p.Ala555Thr
|
|
|
NM_001354693.2:c.1807G>A
(RAF1)
|
NP_001341622.1:p.Ala603Thr
|
|
|
NM_001354694.2:c.1723G>A
(RAF1)
|
NP_001341623.1:p.Ala575Thr
|
|
|
NM_001354695.2:c.1564G>A
(RAF1)
|
NP_001341624.1:p.Ala522Thr
|
|
|
NR_148940.2:n.2350G>A
(RAF1)
|
|
|
|
NR_148941.2:n.2296G>A
(RAF1)
|
|
|
|
NR_148942.2:n.2235G>A
(RAF1)
|
|
|
|
NM_001354690.3:c.1906G>A
(RAF1)
|
NP_001341619.1:p.Ala636Thr
|
|
|
NM_001354691.3:c.1663G>A
(RAF1)
|
NP_001341620.1:p.Ala555Thr
|
|
|
NM_001354692.3:c.1663G>A
(RAF1)
|
NP_001341621.1:p.Ala555Thr
|
|
|
NM_001354693.3:c.1807G>A
(RAF1)
|
NP_001341622.1:p.Ala603Thr
|
|
|
NM_001354694.3:c.1723G>A
(RAF1)
|
NP_001341623.1:p.Ala575Thr
|
|
|
NM_001354695.3:c.1564G>A
(RAF1)
|
NP_001341624.1:p.Ala522Thr
|
|
|
NM_002880.4:c.1906G>A
(RAF1)
MANE Select
|
NP_002871.1:p.Ala636Thr
|
|
|
NR_148940.3:n.2350G>A
(RAF1)
|
|
|
|
NR_148941.3:n.2296G>A
(RAF1)
|
|
|
|
NR_148942.3:n.2235G>A
(RAF1)
|
|
|
