|
ENST00000423275.6:c.*1370G>C
(RAF1)
|
ENSP00000401088.1:n.*1370G>C
|
|
|
ENST00000432427.3:c.1022G>C
(RAF1)
|
|
|
|
ENST00000460610.2:n.6017G>C
(RAF1)
|
|
|
|
ENST00000471449.2:n.515G>C
(RAF1)
|
|
|
|
ENST00000475353.2:n.3985G>C
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1382G>C
(RAF1)
|
ENSP00000508612.1:n.*1382G>C
|
|
|
ENST00000685348.1:c.*1416G>C
(RAF1)
|
ENSP00000510285.1:n.*1416G>C
|
|
|
ENST00000685437.1:c.1606G>C
(RAF1)
|
ENSP00000508794.1:p.Asp536His
|
|
|
ENST00000685653.1:c.1705G>C
(RAF1)
|
ENSP00000509968.1:p.Asp569His
|
|
|
ENST00000685697.1:n.2440G>C
(RAF1)
|
|
|
|
ENST00000685738.1:c.*669G>C
(RAF1)
|
ENSP00000510156.1:n.*669G>C
|
|
|
ENST00000686409.1:n.5114G>C
(RAF1)
|
|
|
|
ENST00000686455.1:n.4426G>C
(RAF1)
|
|
|
|
ENST00000686762.1:c.*264G>C
(RAF1)
|
ENSP00000509767.1:n.*264G>C
|
|
|
ENST00000687257.1:n.4159G>C
(RAF1)
|
|
|
|
ENST00000687326.1:c.*2997G>C
(RAF1)
|
ENSP00000509665.1:n.*2997G>C
|
|
|
ENST00000687505.1:n.1823G>C
(RAF1)
|
|
|
|
ENST00000687923.1:c.1594G>C
(RAF1)
|
ENSP00000510255.1:p.Asp532His
|
|
|
ENST00000688269.1:n.2301G>C
(RAF1)
|
|
|
|
ENST00000688444.1:n.3822G>C
(RAF1)
|
|
|
|
ENST00000688543.1:c.1606G>C
(RAF1)
|
ENSP00000509612.1:p.Asp536His
|
|
|
ENST00000688625.1:c.*3074G>C
(RAF1)
|
ENSP00000509522.1:n.*3074G>C
|
|
|
ENST00000688803.1:n.3133G>C
(RAF1)
|
|
|
|
ENST00000688914.1:n.1118G>C
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1382G>C
(RAF1)
|
ENSP00000509756.1:n.*1382G>C
|
|
|
ENST00000689389.1:c.1528G>C
(RAF1)
|
ENSP00000510213.1:p.Asp510His
|
|
|
ENST00000689418.1:c.*3600G>C
(RAF1)
|
ENSP00000509467.1:n.*3600G>C
|
|
|
ENST00000689540.1:n.4073G>C
(RAF1)
|
|
|
|
ENST00000689876.1:c.*254G>C
(RAF1)
|
ENSP00000508535.1:n.*254G>C
|
|
|
ENST00000689914.1:c.*639G>C
(RAF1)
|
ENSP00000509847.1:n.*639G>C
|
|
|
ENST00000690397.1:c.1594G>C
(RAF1)
|
ENSP00000508730.1:p.Asp532His
|
|
|
ENST00000690460.1:c.1693G>C
(RAF1)
|
ENSP00000509106.1:p.Asp565His
|
|
|
ENST00000690585.1:c.431G>C
(RAF1)
|
|
|
|
ENST00000690625.1:n.2741G>C
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1577G>C
(RAF1)
|
ENSP00000510712.1:n.*1577G>C
|
|
|
ENST00000691643.1:n.2758G>C
(RAF1)
|
|
|
|
ENST00000691724.1:c.*662G>C
(RAF1)
|
ENSP00000509255.1:n.*662G>C
|
|
|
ENST00000691779.1:c.*1283G>C
(RAF1)
|
ENSP00000508592.1:n.*1283G>C
|
|
|
ENST00000691888.1:c.579G>C
(RAF1)
|
|
|
|
ENST00000691899.1:c.1705G>C
(RAF1)
|
ENSP00000508763.1:p.Asp569His
|
|
|
ENST00000692069.1:n.4629G>C
(RAF1)
|
|
|
|
ENST00000692093.1:c.1606G>C
(RAF1)
|
ENSP00000509669.1:p.Asp536His
|
|
|
ENST00000692311.1:n.2529G>C
(RAF1)
|
|
|
|
ENST00000692558.1:n.4288G>C
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1442G>C
(RAF1)
|
ENSP00000509055.1:n.*1442G>C
|
|
|
ENST00000692830.1:c.*1450G>C
(RAF1)
|
ENSP00000509461.1:n.*1450G>C
|
|
|
ENST00000693312.1:c.1480G>C
(RAF1)
|
ENSP00000508686.1:p.Asp494His
|
|
|
ENST00000693664.1:c.*156G>C
(RAF1)
|
ENSP00000509614.1:n.*156G>C
|
|
|
ENST00000693705.1:c.*1084G>C
(RAF1)
|
ENSP00000510697.1:n.*1084G>C
|
|
|
ENST00000251849.9:c.1705G>C
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Asp569His
|
|
|
ENST00000442415.7:c.1765G>C
(RAF1)
|
ENSP00000401888.2:p.Asp589His
|
|
|
ENST00000676541.1:c.*2692C>G
(MKRN2)
|
ENSP00000503730.1:n.*2692C>G
|
|
|
ENST00000677142.1:c.*2692C>G
(MKRN2)
|
ENSP00000504455.1:n.*2692C>G
|
|
|
ENST00000677816.1:c.*1247C>G
(MKRN2)
|
ENSP00000502893.1:n.*1247C>G
|
|
|
ENST00000677941.1:n.2755C>G
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1705G>C
(RAF1)
|
ENSP00000251849.4:p.Asp569His
|
|
|
ENST00000423275.5:c.*1382G>C
(RAF1)
|
ENSP00000401088.1:n.*1382G>C
|
|
|
ENST00000432427.2:c.1342G>C
(RAF1)
|
ENSP00000398591.2:p.Asp448His
|
|
|
ENST00000442415.6:c.1765G>C
(RAF1)
|
ENSP00000401888.2:p.Asp589His
|
|
|
ENST00000471449.1:n.394G>C
(RAF1)
|
|
|
|
NM_002880.3:c.1705G>C , LRG_413t1:c.1705G>C
(RAF1)
|
NP_002871.1:p.Asp569His
|
|
|
XM_005265355.1:c.1705G>C
(RAF1)
|
XP_005265412.1:p.Asp569His
|
|
|
XM_005265357.1:c.1606G>C
(RAF1)
|
XP_005265414.1:p.Asp536His
|
|
|
XM_005265358.3:c.1462G>C
(RAF1)
|
XP_005265415.1:p.Asp488His
|
|
|
XM_005265359.3:c.1363G>C
(RAF1)
|
XP_005265416.1:p.Asp455His
|
|
|
XM_011533974.1:c.1705G>C
(RAF1)
|
XP_011532276.1:p.Asp569His
|
|
|
XM_011533975.1:c.1462G>C
(RAF1)
|
XP_011532277.1:p.Asp488His
|
|
|
NM_001354689.1:c.1765G>C
(RAF1)
|
NP_001341618.1:p.Asp589His
|
|
|
NM_001354690.1:c.1705G>C
(RAF1)
|
NP_001341619.1:p.Asp569His
|
|
|
NM_001354691.1:c.1462G>C
(RAF1)
|
NP_001341620.1:p.Asp488His
|
|
|
NM_001354692.1:c.1462G>C
(RAF1)
|
NP_001341621.1:p.Asp488His
|
|
|
NM_001354693.1:c.1606G>C
(RAF1)
|
NP_001341622.1:p.Asp536His
|
|
|
NM_001354694.1:c.1522G>C
(RAF1)
|
NP_001341623.1:p.Asp508His
|
|
|
NM_001354695.1:c.1363G>C
(RAF1)
|
NP_001341624.1:p.Asp455His
|
|
|
NR_148940.1:n.2233G>C
(RAF1)
|
|
|
|
NR_148941.1:n.2179G>C
(RAF1)
|
|
|
|
NR_148942.1:n.2118G>C
(RAF1)
|
|
|
|
XM_011533974.3:c.1705G>C
(RAF1)
|
XP_011532276.1:p.Asp569His
|
|
|
XM_017006966.1:c.1606G>C
(RAF1)
|
XP_016862455.1:p.Asp536His
|
|
|
NM_001354689.3:c.1765G>C
(RAF1)
|
NP_001341618.1:p.Asp589His
|
|
|
NM_001354690.2:c.1705G>C
(RAF1)
|
NP_001341619.1:p.Asp569His
|
|
|
NM_001354691.2:c.1462G>C
(RAF1)
|
NP_001341620.1:p.Asp488His
|
|
|
NM_001354692.2:c.1462G>C
(RAF1)
|
NP_001341621.1:p.Asp488His
|
|
|
NM_001354693.2:c.1606G>C
(RAF1)
|
NP_001341622.1:p.Asp536His
|
|
|
NM_001354694.2:c.1522G>C
(RAF1)
|
NP_001341623.1:p.Asp508His
|
|
|
NM_001354695.2:c.1363G>C
(RAF1)
|
NP_001341624.1:p.Asp455His
|
|
|
NR_148940.2:n.2149G>C
(RAF1)
|
|
|
|
NR_148941.2:n.2095G>C
(RAF1)
|
|
|
|
NR_148942.2:n.2034G>C
(RAF1)
|
|
|
|
NM_001354690.3:c.1705G>C
(RAF1)
|
NP_001341619.1:p.Asp569His
|
|
|
NM_001354691.3:c.1462G>C
(RAF1)
|
NP_001341620.1:p.Asp488His
|
|
|
NM_001354692.3:c.1462G>C
(RAF1)
|
NP_001341621.1:p.Asp488His
|
|
|
NM_001354693.3:c.1606G>C
(RAF1)
|
NP_001341622.1:p.Asp536His
|
|
|
NM_001354694.3:c.1522G>C
(RAF1)
|
NP_001341623.1:p.Asp508His
|
|
|
NM_001354695.3:c.1363G>C
(RAF1)
|
NP_001341624.1:p.Asp455His
|
|
|
NM_002880.4:c.1705G>C
(RAF1)
MANE Select
|
NP_002871.1:p.Asp569His
|
|
|
NR_148940.3:n.2149G>C
(RAF1)
|
|
|
|
NR_148941.3:n.2095G>C
(RAF1)
|
|
|
|
NR_148942.3:n.2034G>C
(RAF1)
|
|
|
