|
ENST00000423275.6:c.*1453G>T
(RAF1)
|
ENSP00000401088.1:n.*1453G>T
|
|
|
ENST00000432427.3:c.1105G>T
(RAF1)
|
|
|
|
ENST00000460610.2:n.6100G>T
(RAF1)
|
|
|
|
ENST00000471449.2:n.598G>T
(RAF1)
|
|
|
|
ENST00000475353.2:n.4068G>T
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1465G>T
(RAF1)
|
ENSP00000508612.1:n.*1465G>T
|
|
|
ENST00000685348.1:c.*1499G>T
(RAF1)
|
ENSP00000510285.1:n.*1499G>T
|
|
|
ENST00000685437.1:c.1689G>T
(RAF1)
|
ENSP00000508794.1:p.Arg563Ser
|
|
|
ENST00000685653.1:c.1788G>T
(RAF1)
|
ENSP00000509968.1:p.Arg596Ser
|
|
|
ENST00000685697.1:n.2523G>T
(RAF1)
|
|
|
|
ENST00000685738.1:c.*752G>T
(RAF1)
|
ENSP00000510156.1:n.*752G>T
|
|
|
ENST00000686409.1:n.5197G>T
(RAF1)
|
|
|
|
ENST00000686455.1:n.4509G>T
(RAF1)
|
|
|
|
ENST00000686762.1:c.*347G>T
(RAF1)
|
ENSP00000509767.1:n.*347G>T
|
|
|
ENST00000687257.1:n.4242G>T
(RAF1)
|
|
|
|
ENST00000687326.1:c.*3080G>T
(RAF1)
|
ENSP00000509665.1:n.*3080G>T
|
|
|
ENST00000687505.1:n.1906G>T
(RAF1)
|
|
|
|
ENST00000687923.1:c.1677G>T
(RAF1)
|
ENSP00000510255.1:p.Arg559Ser
|
|
|
ENST00000688269.1:n.2384G>T
(RAF1)
|
|
|
|
ENST00000688444.1:n.3905G>T
(RAF1)
|
|
|
|
ENST00000688543.1:c.1689G>T
(RAF1)
|
ENSP00000509612.1:p.Arg563Ser
|
|
|
ENST00000688625.1:c.*3157G>T
(RAF1)
|
ENSP00000509522.1:n.*3157G>T
|
|
|
ENST00000688803.1:n.3216G>T
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1465G>T
(RAF1)
|
ENSP00000509756.1:n.*1465G>T
|
|
|
ENST00000689389.1:c.1611G>T
(RAF1)
|
ENSP00000510213.1:p.Arg537Ser
|
|
|
ENST00000689418.1:c.*3683G>T
(RAF1)
|
ENSP00000509467.1:n.*3683G>T
|
|
|
ENST00000689540.1:n.4156G>T
(RAF1)
|
|
|
|
ENST00000689876.1:c.*337G>T
(RAF1)
|
ENSP00000508535.1:n.*337G>T
|
|
|
ENST00000689914.1:c.*722G>T
(RAF1)
|
ENSP00000509847.1:n.*722G>T
|
|
|
ENST00000690397.1:c.1677G>T
(RAF1)
|
ENSP00000508730.1:p.Arg559Ser
|
|
|
ENST00000690460.1:c.1776G>T
(RAF1)
|
ENSP00000509106.1:p.Arg592Ser
|
|
|
ENST00000690585.1:c.514G>T
(RAF1)
|
|
|
|
ENST00000690625.1:n.2824G>T
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1660G>T
(RAF1)
|
ENSP00000510712.1:n.*1660G>T
|
|
|
ENST00000691643.1:n.2841G>T
(RAF1)
|
|
|
|
ENST00000691724.1:c.*745G>T
(RAF1)
|
ENSP00000509255.1:n.*745G>T
|
|
|
ENST00000691779.1:c.*1366G>T
(RAF1)
|
ENSP00000508592.1:n.*1366G>T
|
|
|
ENST00000691888.1:c.662G>T
(RAF1)
|
|
|
|
ENST00000691899.1:c.1788G>T
(RAF1)
|
ENSP00000508763.1:p.Arg596Ser
|
|
|
ENST00000692069.1:n.4712G>T
(RAF1)
|
|
|
|
ENST00000692093.1:c.1689G>T
(RAF1)
|
ENSP00000509669.1:p.Arg563Ser
|
|
|
ENST00000692311.1:n.2612G>T
(RAF1)
|
|
|
|
ENST00000692558.1:n.4371G>T
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1525G>T
(RAF1)
|
ENSP00000509055.1:n.*1525G>T
|
|
|
ENST00000692830.1:c.*1533G>T
(RAF1)
|
ENSP00000509461.1:n.*1533G>T
|
|
|
ENST00000693312.1:c.1563G>T
(RAF1)
|
ENSP00000508686.1:p.Arg521Ser
|
|
|
ENST00000693664.1:c.*239G>T
(RAF1)
|
ENSP00000509614.1:n.*239G>T
|
|
|
ENST00000693705.1:c.*1167G>T
(RAF1)
|
ENSP00000510697.1:n.*1167G>T
|
|
|
ENST00000251849.9:c.1788G>T
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Arg596Ser
|
|
|
ENST00000442415.7:c.1848G>T
(RAF1)
|
ENSP00000401888.2:p.Arg616Ser
|
|
|
ENST00000676541.1:c.*2609C>A
(MKRN2)
|
ENSP00000503730.1:n.*2609C>A
|
|
|
ENST00000677142.1:c.*2609C>A
(MKRN2)
|
ENSP00000504455.1:n.*2609C>A
|
|
|
ENST00000677816.1:c.*1164C>A
(MKRN2)
|
ENSP00000502893.1:n.*1164C>A
|
|
|
ENST00000677941.1:n.2672C>A
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1788G>T
(RAF1)
|
ENSP00000251849.4:p.Arg596Ser
|
|
|
ENST00000423275.5:c.*1465G>T
(RAF1)
|
ENSP00000401088.1:n.*1465G>T
|
|
|
ENST00000432427.2:c.1425G>T
(RAF1)
|
ENSP00000398591.2:p.Arg475Ser
|
|
|
ENST00000442415.6:c.1848G>T
(RAF1)
|
ENSP00000401888.2:p.Arg616Ser
|
|
|
ENST00000471449.1:n.477G>T
(RAF1)
|
|
|
|
NM_002880.3:c.1788G>T , LRG_413t1:c.1788G>T
(RAF1)
|
NP_002871.1:p.Arg596Ser
|
|
|
XM_005265355.1:c.1788G>T
(RAF1)
|
XP_005265412.1:p.Arg596Ser
|
|
|
XM_005265357.1:c.1689G>T
(RAF1)
|
XP_005265414.1:p.Arg563Ser
|
|
|
XM_005265358.3:c.1545G>T
(RAF1)
|
XP_005265415.1:p.Arg515Ser
|
|
|
XM_005265359.3:c.1446G>T
(RAF1)
|
XP_005265416.1:p.Arg482Ser
|
|
|
XM_011533974.1:c.1788G>T
(RAF1)
|
XP_011532276.1:p.Arg596Ser
|
|
|
XM_011533975.1:c.1545G>T
(RAF1)
|
XP_011532277.1:p.Arg515Ser
|
|
|
NM_001354689.1:c.1848G>T
(RAF1)
|
NP_001341618.1:p.Arg616Ser
|
|
|
NM_001354690.1:c.1788G>T
(RAF1)
|
NP_001341619.1:p.Arg596Ser
|
|
|
NM_001354691.1:c.1545G>T
(RAF1)
|
NP_001341620.1:p.Arg515Ser
|
|
|
NM_001354692.1:c.1545G>T
(RAF1)
|
NP_001341621.1:p.Arg515Ser
|
|
|
NM_001354693.1:c.1689G>T
(RAF1)
|
NP_001341622.1:p.Arg563Ser
|
|
|
NM_001354694.1:c.1605G>T
(RAF1)
|
NP_001341623.1:p.Arg535Ser
|
|
|
NM_001354695.1:c.1446G>T
(RAF1)
|
NP_001341624.1:p.Arg482Ser
|
|
|
NR_148940.1:n.2316G>T
(RAF1)
|
|
|
|
NR_148941.1:n.2262G>T
(RAF1)
|
|
|
|
NR_148942.1:n.2201G>T
(RAF1)
|
|
|
|
XM_011533974.3:c.1788G>T
(RAF1)
|
XP_011532276.1:p.Arg596Ser
|
|
|
XM_017006966.1:c.1689G>T
(RAF1)
|
XP_016862455.1:p.Arg563Ser
|
|
|
NM_001354689.3:c.1848G>T
(RAF1)
|
NP_001341618.1:p.Arg616Ser
|
|
|
NM_001354690.2:c.1788G>T
(RAF1)
|
NP_001341619.1:p.Arg596Ser
|
|
|
NM_001354691.2:c.1545G>T
(RAF1)
|
NP_001341620.1:p.Arg515Ser
|
|
|
NM_001354692.2:c.1545G>T
(RAF1)
|
NP_001341621.1:p.Arg515Ser
|
|
|
NM_001354693.2:c.1689G>T
(RAF1)
|
NP_001341622.1:p.Arg563Ser
|
|
|
NM_001354694.2:c.1605G>T
(RAF1)
|
NP_001341623.1:p.Arg535Ser
|
|
|
NM_001354695.2:c.1446G>T
(RAF1)
|
NP_001341624.1:p.Arg482Ser
|
|
|
NR_148940.2:n.2232G>T
(RAF1)
|
|
|
|
NR_148941.2:n.2178G>T
(RAF1)
|
|
|
|
NR_148942.2:n.2117G>T
(RAF1)
|
|
|
|
NM_001354690.3:c.1788G>T
(RAF1)
|
NP_001341619.1:p.Arg596Ser
|
|
|
NM_001354691.3:c.1545G>T
(RAF1)
|
NP_001341620.1:p.Arg515Ser
|
|
|
NM_001354692.3:c.1545G>T
(RAF1)
|
NP_001341621.1:p.Arg515Ser
|
|
|
NM_001354693.3:c.1689G>T
(RAF1)
|
NP_001341622.1:p.Arg563Ser
|
|
|
NM_001354694.3:c.1605G>T
(RAF1)
|
NP_001341623.1:p.Arg535Ser
|
|
|
NM_001354695.3:c.1446G>T
(RAF1)
|
NP_001341624.1:p.Arg482Ser
|
|
|
NM_002880.4:c.1788G>T
(RAF1)
MANE Select
|
NP_002871.1:p.Arg596Ser
|
|
|
NR_148940.3:n.2232G>T
(RAF1)
|
|
|
|
NR_148941.3:n.2178G>T
(RAF1)
|
|
|
|
NR_148942.3:n.2117G>T
(RAF1)
|
|
|
