|
ENST00000423275.6:c.*1350G>C
(RAF1)
|
ENSP00000401088.1:n.*1350G>C
|
|
|
ENST00000432427.3:c.1002G>C
(RAF1)
|
|
|
|
ENST00000460610.2:n.5997G>C
(RAF1)
|
|
|
|
ENST00000471449.2:n.495G>C
(RAF1)
|
|
|
|
ENST00000475353.2:n.3965G>C
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1362G>C
(RAF1)
|
ENSP00000508612.1:n.*1362G>C
|
|
|
ENST00000685348.1:c.*1396G>C
(RAF1)
|
ENSP00000510285.1:n.*1396G>C
|
|
|
ENST00000685437.1:c.1586G>C
(RAF1)
|
ENSP00000508794.1:p.Gly529Ala
|
|
|
ENST00000685653.1:c.1685G>C
(RAF1)
|
ENSP00000509968.1:p.Gly562Ala
|
|
|
ENST00000685697.1:n.2420G>C
(RAF1)
|
|
|
|
ENST00000685738.1:c.*649G>C
(RAF1)
|
ENSP00000510156.1:n.*649G>C
|
|
|
ENST00000686409.1:n.5094G>C
(RAF1)
|
|
|
|
ENST00000686455.1:n.4406G>C
(RAF1)
|
|
|
|
ENST00000686762.1:c.*244G>C
(RAF1)
|
ENSP00000509767.1:n.*244G>C
|
|
|
ENST00000687257.1:n.4139G>C
(RAF1)
|
|
|
|
ENST00000687326.1:c.*2977G>C
(RAF1)
|
ENSP00000509665.1:n.*2977G>C
|
|
|
ENST00000687505.1:n.1803G>C
(RAF1)
|
|
|
|
ENST00000687923.1:c.1574G>C
(RAF1)
|
ENSP00000510255.1:p.Gly525Ala
|
|
|
ENST00000688269.1:n.2281G>C
(RAF1)
|
|
|
|
ENST00000688444.1:n.3802G>C
(RAF1)
|
|
|
|
ENST00000688543.1:c.1586G>C
(RAF1)
|
ENSP00000509612.1:p.Gly529Ala
|
|
|
ENST00000688625.1:c.*3054G>C
(RAF1)
|
ENSP00000509522.1:n.*3054G>C
|
|
|
ENST00000688803.1:n.3113G>C
(RAF1)
|
|
|
|
ENST00000688914.1:n.1098G>C
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1362G>C
(RAF1)
|
ENSP00000509756.1:n.*1362G>C
|
|
|
ENST00000689389.1:c.1508G>C
(RAF1)
|
ENSP00000510213.1:p.Gly503Ala
|
|
|
ENST00000689418.1:c.*3580G>C
(RAF1)
|
ENSP00000509467.1:n.*3580G>C
|
|
|
ENST00000689540.1:n.4053G>C
(RAF1)
|
|
|
|
ENST00000689876.1:c.*234G>C
(RAF1)
|
ENSP00000508535.1:n.*234G>C
|
|
|
ENST00000689914.1:c.*619G>C
(RAF1)
|
ENSP00000509847.1:n.*619G>C
|
|
|
ENST00000690397.1:c.1574G>C
(RAF1)
|
ENSP00000508730.1:p.Gly525Ala
|
|
|
ENST00000690460.1:c.1673G>C
(RAF1)
|
ENSP00000509106.1:p.Gly558Ala
|
|
|
ENST00000690585.1:c.411G>C
(RAF1)
|
|
|
|
ENST00000690625.1:n.2721G>C
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1557G>C
(RAF1)
|
ENSP00000510712.1:n.*1557G>C
|
|
|
ENST00000691643.1:n.2738G>C
(RAF1)
|
|
|
|
ENST00000691724.1:c.*642G>C
(RAF1)
|
ENSP00000509255.1:n.*642G>C
|
|
|
ENST00000691779.1:c.*1263G>C
(RAF1)
|
ENSP00000508592.1:n.*1263G>C
|
|
|
ENST00000691888.1:c.559G>C
(RAF1)
|
|
|
|
ENST00000691899.1:c.1685G>C
(RAF1)
|
ENSP00000508763.1:p.Gly562Ala
|
|
|
ENST00000692069.1:n.4609G>C
(RAF1)
|
|
|
|
ENST00000692093.1:c.1586G>C
(RAF1)
|
ENSP00000509669.1:p.Gly529Ala
|
|
|
ENST00000692311.1:n.2509G>C
(RAF1)
|
|
|
|
ENST00000692558.1:n.4268G>C
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1422G>C
(RAF1)
|
ENSP00000509055.1:n.*1422G>C
|
|
|
ENST00000692830.1:c.*1430G>C
(RAF1)
|
ENSP00000509461.1:n.*1430G>C
|
|
|
ENST00000693312.1:c.1460G>C
(RAF1)
|
ENSP00000508686.1:p.Gly487Ala
|
|
|
ENST00000693664.1:c.*136G>C
(RAF1)
|
ENSP00000509614.1:n.*136G>C
|
|
|
ENST00000693705.1:c.*1064G>C
(RAF1)
|
ENSP00000510697.1:n.*1064G>C
|
|
|
ENST00000251849.9:c.1685G>C
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Gly562Ala
|
|
|
ENST00000442415.7:c.1745G>C
(RAF1)
|
ENSP00000401888.2:p.Gly582Ala
|
|
|
ENST00000676541.1:c.*2712C>G
(MKRN2)
|
ENSP00000503730.1:n.*2712C>G
|
|
|
ENST00000677142.1:c.*2712C>G
(MKRN2)
|
ENSP00000504455.1:n.*2712C>G
|
|
|
ENST00000677816.1:c.*1267C>G
(MKRN2)
|
ENSP00000502893.1:n.*1267C>G
|
|
|
ENST00000677941.1:n.2775C>G
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1685G>C
(RAF1)
|
ENSP00000251849.4:p.Gly562Ala
|
|
|
ENST00000423275.5:c.*1362G>C
(RAF1)
|
ENSP00000401088.1:n.*1362G>C
|
|
|
ENST00000432427.2:c.1322G>C
(RAF1)
|
ENSP00000398591.2:p.Gly441Ala
|
|
|
ENST00000442415.6:c.1745G>C
(RAF1)
|
ENSP00000401888.2:p.Gly582Ala
|
|
|
ENST00000471449.1:n.374G>C
(RAF1)
|
|
|
|
NM_002880.3:c.1685G>C , LRG_413t1:c.1685G>C
(RAF1)
|
NP_002871.1:p.Gly562Ala
|
|
|
XM_005265355.1:c.1685G>C
(RAF1)
|
XP_005265412.1:p.Gly562Ala
|
|
|
XM_005265357.1:c.1586G>C
(RAF1)
|
XP_005265414.1:p.Gly529Ala
|
|
|
XM_005265358.3:c.1442G>C
(RAF1)
|
XP_005265415.1:p.Gly481Ala
|
|
|
XM_005265359.3:c.1343G>C
(RAF1)
|
XP_005265416.1:p.Gly448Ala
|
|
|
XM_011533974.1:c.1685G>C
(RAF1)
|
XP_011532276.1:p.Gly562Ala
|
|
|
XM_011533975.1:c.1442G>C
(RAF1)
|
XP_011532277.1:p.Gly481Ala
|
|
|
NM_001354689.1:c.1745G>C
(RAF1)
|
NP_001341618.1:p.Gly582Ala
|
|
|
NM_001354690.1:c.1685G>C
(RAF1)
|
NP_001341619.1:p.Gly562Ala
|
|
|
NM_001354691.1:c.1442G>C
(RAF1)
|
NP_001341620.1:p.Gly481Ala
|
|
|
NM_001354692.1:c.1442G>C
(RAF1)
|
NP_001341621.1:p.Gly481Ala
|
|
|
NM_001354693.1:c.1586G>C
(RAF1)
|
NP_001341622.1:p.Gly529Ala
|
|
|
NM_001354694.1:c.1502G>C
(RAF1)
|
NP_001341623.1:p.Gly501Ala
|
|
|
NM_001354695.1:c.1343G>C
(RAF1)
|
NP_001341624.1:p.Gly448Ala
|
|
|
NR_148940.1:n.2213G>C
(RAF1)
|
|
|
|
NR_148941.1:n.2159G>C
(RAF1)
|
|
|
|
NR_148942.1:n.2098G>C
(RAF1)
|
|
|
|
XM_011533974.3:c.1685G>C
(RAF1)
|
XP_011532276.1:p.Gly562Ala
|
|
|
XM_017006966.1:c.1586G>C
(RAF1)
|
XP_016862455.1:p.Gly529Ala
|
|
|
NM_001354689.3:c.1745G>C
(RAF1)
|
NP_001341618.1:p.Gly582Ala
|
|
|
NM_001354690.2:c.1685G>C
(RAF1)
|
NP_001341619.1:p.Gly562Ala
|
|
|
NM_001354691.2:c.1442G>C
(RAF1)
|
NP_001341620.1:p.Gly481Ala
|
|
|
NM_001354692.2:c.1442G>C
(RAF1)
|
NP_001341621.1:p.Gly481Ala
|
|
|
NM_001354693.2:c.1586G>C
(RAF1)
|
NP_001341622.1:p.Gly529Ala
|
|
|
NM_001354694.2:c.1502G>C
(RAF1)
|
NP_001341623.1:p.Gly501Ala
|
|
|
NM_001354695.2:c.1343G>C
(RAF1)
|
NP_001341624.1:p.Gly448Ala
|
|
|
NR_148940.2:n.2129G>C
(RAF1)
|
|
|
|
NR_148941.2:n.2075G>C
(RAF1)
|
|
|
|
NR_148942.2:n.2014G>C
(RAF1)
|
|
|
|
NM_001354690.3:c.1685G>C
(RAF1)
|
NP_001341619.1:p.Gly562Ala
|
|
|
NM_001354691.3:c.1442G>C
(RAF1)
|
NP_001341620.1:p.Gly481Ala
|
|
|
NM_001354692.3:c.1442G>C
(RAF1)
|
NP_001341621.1:p.Gly481Ala
|
|
|
NM_001354693.3:c.1586G>C
(RAF1)
|
NP_001341622.1:p.Gly529Ala
|
|
|
NM_001354694.3:c.1502G>C
(RAF1)
|
NP_001341623.1:p.Gly501Ala
|
|
|
NM_001354695.3:c.1343G>C
(RAF1)
|
NP_001341624.1:p.Gly448Ala
|
|
|
NM_002880.4:c.1685G>C
(RAF1)
MANE Select
|
NP_002871.1:p.Gly562Ala
|
|
|
NR_148940.3:n.2129G>C
(RAF1)
|
|
|
|
NR_148941.3:n.2075G>C
(RAF1)
|
|
|
|
NR_148942.3:n.2014G>C
(RAF1)
|
|
|
