|
ENST00000423275.6:c.*1098A>T
(RAF1)
|
ENSP00000401088.1:n.*1098A>T
|
|
|
ENST00000432427.3:c.750A>T
(RAF1)
|
|
|
|
ENST00000460610.2:n.5178A>T
(RAF1)
|
|
|
|
ENST00000471449.2:n.243A>T
(RAF1)
|
|
|
|
ENST00000475353.2:n.3146A>T
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1110A>T
(RAF1)
|
ENSP00000508612.1:n.*1110A>T
|
|
|
ENST00000685348.1:c.*1095-378A>T
(RAF1)
|
ENSP00000510285.1:n.*1095-378A>T
|
|
|
ENST00000685437.1:c.1334A>T
(RAF1)
|
ENSP00000508794.1:p.Glu445Val
|
|
|
ENST00000685653.1:c.1433A>T
(RAF1)
|
ENSP00000509968.1:p.Glu478Val
|
|
|
ENST00000685697.1:n.2168A>T
(RAF1)
|
|
|
|
ENST00000685738.1:c.*397A>T
(RAF1)
|
ENSP00000510156.1:n.*397A>T
|
|
|
ENST00000686409.1:n.4275A>T
(RAF1)
|
|
|
|
ENST00000686455.1:n.3587A>T
(RAF1)
|
|
|
|
ENST00000686762.1:c.1453A>T
(RAF1)
|
ENSP00000509767.1:p.Lys485Ter
|
|
|
ENST00000687257.1:n.3460A>T
(RAF1)
|
|
|
|
ENST00000687326.1:c.*2158A>T
(RAF1)
|
ENSP00000509665.1:n.*2158A>T
|
|
|
ENST00000687505.1:n.1551A>T
(RAF1)
|
|
|
|
ENST00000687923.1:c.1322A>T
(RAF1)
|
ENSP00000510255.1:p.Glu441Val
|
|
|
ENST00000688269.1:n.2029A>T
(RAF1)
|
|
|
|
ENST00000688444.1:n.3550A>T
(RAF1)
|
|
|
|
ENST00000688543.1:c.1334A>T
(RAF1)
|
ENSP00000509612.1:p.Glu445Val
|
|
|
ENST00000688625.1:c.*2802A>T
(RAF1)
|
ENSP00000509522.1:n.*2802A>T
|
|
|
ENST00000688803.1:n.2964+491A>T
(RAF1)
|
|
|
|
ENST00000688914.1:n.419A>T
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1110A>T
(RAF1)
|
ENSP00000509756.1:n.*1110A>T
|
|
|
ENST00000689389.1:c.1256A>T
(RAF1)
|
ENSP00000510213.1:p.Glu419Val
|
|
|
ENST00000689418.1:c.*2901A>T
(RAF1)
|
ENSP00000509467.1:n.*2901A>T
|
|
|
ENST00000689540.1:n.3374A>T
(RAF1)
|
|
|
|
ENST00000689876.1:c.1418-378A>T
(RAF1)
|
ENSP00000508535.1:n.1418-378A>T
|
|
|
ENST00000689914.1:c.*367A>T
(RAF1)
|
ENSP00000509847.1:n.*367A>T
|
|
|
ENST00000690397.1:c.1322A>T
(RAF1)
|
ENSP00000508730.1:p.Glu441Val
|
|
|
ENST00000690460.1:c.1421A>T
(RAF1)
|
ENSP00000509106.1:p.Glu474Val
|
|
|
ENST00000690585.1:c.263-531A>T
(RAF1)
|
|
|
|
ENST00000690625.1:n.2469A>T
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1305A>T
(RAF1)
|
ENSP00000510712.1:n.*1305A>T
|
|
|
ENST00000691643.1:n.2059A>T
(RAF1)
|
|
|
|
ENST00000691724.1:c.*390A>T
(RAF1)
|
ENSP00000509255.1:n.*390A>T
|
|
|
ENST00000691779.1:c.*1011A>T
(RAF1)
|
ENSP00000508592.1:n.*1011A>T
|
|
|
ENST00000691888.1:c.310-3A>T
(RAF1)
|
|
|
|
ENST00000691899.1:c.1433A>T
(RAF1)
|
ENSP00000508763.1:p.Glu478Val
|
|
|
ENST00000692069.1:n.3790A>T
(RAF1)
|
|
|
|
ENST00000692093.1:c.1334A>T
(RAF1)
|
ENSP00000509669.1:p.Glu445Val
|
|
|
ENST00000692311.1:n.2257A>T
(RAF1)
|
|
|
|
ENST00000692558.1:n.3589A>T
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1170A>T
(RAF1)
|
ENSP00000509055.1:n.*1170A>T
|
|
|
ENST00000692830.1:c.*1178A>T
(RAF1)
|
ENSP00000509461.1:n.*1178A>T
|
|
|
ENST00000693312.1:c.1208A>T
(RAF1)
|
ENSP00000508686.1:p.Glu403Val
|
|
|
ENST00000693664.1:c.1487+491A>T
(RAF1)
|
ENSP00000509614.1:n.1487+491A>T
|
|
|
ENST00000693705.1:c.*1048-803A>T
(RAF1)
|
ENSP00000510697.1:n.*1048-803A>T
|
|
|
ENST00000251849.9:c.1433A>T
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Glu478Val
|
|
|
ENST00000442415.7:c.1493A>T
(RAF1)
|
ENSP00000401888.2:p.Glu498Val
|
|
|
ENST00000676541.1:c.*3531T>A
(MKRN2)
|
ENSP00000503730.1:n.*3531T>A
|
|
|
ENST00000677142.1:c.*3531T>A
(MKRN2)
|
ENSP00000504455.1:n.*3531T>A
|
|
|
ENST00000677816.1:c.*2086T>A
(MKRN2)
|
ENSP00000502893.1:n.*2086T>A
|
|
|
ENST00000677941.1:n.3594T>A
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1433A>T
(RAF1)
|
ENSP00000251849.4:p.Glu478Val
|
|
|
ENST00000423275.5:c.*1110A>T
(RAF1)
|
ENSP00000401088.1:n.*1110A>T
|
|
|
ENST00000432427.2:c.1070A>T
(RAF1)
|
ENSP00000398591.2:p.Glu357Val
|
|
|
ENST00000442415.6:c.1493A>T
(RAF1)
|
ENSP00000401888.2:p.Glu498Val
|
|
|
ENST00000471449.1:n.122A>T
(RAF1)
|
|
|
|
NM_002880.3:c.1433A>T , LRG_413t1:c.1433A>T
(RAF1)
|
NP_002871.1:p.Glu478Val
|
|
|
XM_005265355.1:c.1433A>T
(RAF1)
|
XP_005265412.1:p.Glu478Val
|
|
|
XM_005265357.1:c.1334A>T
(RAF1)
|
XP_005265414.1:p.Glu445Val
|
|
|
XM_005265358.3:c.1190A>T
(RAF1)
|
XP_005265415.1:p.Glu397Val
|
|
|
XM_005265359.3:c.1091A>T
(RAF1)
|
XP_005265416.1:p.Glu364Val
|
|
|
XM_005265360.1:c.1418-378A>T
(RAF1)
|
XP_005265417.1:n.1418-378A>T
|
|
|
XM_011533974.1:c.1433A>T
(RAF1)
|
XP_011532276.1:p.Glu478Val
|
|
|
XM_011533975.1:c.1190A>T
(RAF1)
|
XP_011532277.1:p.Glu397Val
|
|
|
NM_001354689.1:c.1493A>T
(RAF1)
|
NP_001341618.1:p.Glu498Val
|
|
|
NM_001354690.1:c.1433A>T
(RAF1)
|
NP_001341619.1:p.Glu478Val
|
|
|
NM_001354691.1:c.1190A>T
(RAF1)
|
NP_001341620.1:p.Glu397Val
|
|
|
NM_001354692.1:c.1190A>T
(RAF1)
|
NP_001341621.1:p.Glu397Val
|
|
|
NM_001354693.1:c.1334A>T
(RAF1)
|
NP_001341622.1:p.Glu445Val
|
|
|
NM_001354694.1:c.1250A>T
(RAF1)
|
NP_001341623.1:p.Glu417Val
|
|
|
NM_001354695.1:c.1091A>T
(RAF1)
|
NP_001341624.1:p.Glu364Val
|
|
|
NR_148940.1:n.1961A>T
(RAF1)
|
|
|
|
NR_148941.1:n.1907A>T
(RAF1)
|
|
|
|
NR_148942.1:n.1846A>T
(RAF1)
|
|
|
|
XM_011533974.3:c.1433A>T
(RAF1)
|
XP_011532276.1:p.Glu478Val
|
|
|
XM_017006966.1:c.1334A>T
(RAF1)
|
XP_016862455.1:p.Glu445Val
|
|
|
NM_001354689.3:c.1493A>T
(RAF1)
|
NP_001341618.1:p.Glu498Val
|
|
|
NM_001354690.2:c.1433A>T
(RAF1)
|
NP_001341619.1:p.Glu478Val
|
|
|
NM_001354691.2:c.1190A>T
(RAF1)
|
NP_001341620.1:p.Glu397Val
|
|
|
NM_001354692.2:c.1190A>T
(RAF1)
|
NP_001341621.1:p.Glu397Val
|
|
|
NM_001354693.2:c.1334A>T
(RAF1)
|
NP_001341622.1:p.Glu445Val
|
|
|
NM_001354694.2:c.1250A>T
(RAF1)
|
NP_001341623.1:p.Glu417Val
|
|
|
NM_001354695.2:c.1091A>T
(RAF1)
|
NP_001341624.1:p.Glu364Val
|
|
|
NR_148940.2:n.1877A>T
(RAF1)
|
|
|
|
NR_148941.2:n.1823A>T
(RAF1)
|
|
|
|
NR_148942.2:n.1762A>T
(RAF1)
|
|
|
|
NM_001354690.3:c.1433A>T
(RAF1)
|
NP_001341619.1:p.Glu478Val
|
|
|
NM_001354691.3:c.1190A>T
(RAF1)
|
NP_001341620.1:p.Glu397Val
|
|
|
NM_001354692.3:c.1190A>T
(RAF1)
|
NP_001341621.1:p.Glu397Val
|
|
|
NM_001354693.3:c.1334A>T
(RAF1)
|
NP_001341622.1:p.Glu445Val
|
|
|
NM_001354694.3:c.1250A>T
(RAF1)
|
NP_001341623.1:p.Glu417Val
|
|
|
NM_001354695.3:c.1091A>T
(RAF1)
|
NP_001341624.1:p.Glu364Val
|
|
|
NM_002880.4:c.1433A>T
(RAF1)
MANE Select
|
NP_002871.1:p.Glu478Val
|
|
|
NR_148940.3:n.1877A>T
(RAF1)
|
|
|
|
NR_148941.3:n.1823A>T
(RAF1)
|
|
|
|
NR_148942.3:n.1762A>T
(RAF1)
|
|
|
