|
ENST00000423275.6:c.*1459T>C
(RAF1)
|
ENSP00000401088.1:n.*1459T>C
|
|
|
ENST00000432427.3:c.1111T>C
(RAF1)
|
|
|
|
ENST00000460610.2:n.6106T>C
(RAF1)
|
|
|
|
ENST00000471449.2:n.604T>C
(RAF1)
|
|
|
|
ENST00000475353.2:n.4074T>C
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1471T>C
(RAF1)
|
ENSP00000508612.1:n.*1471T>C
|
|
|
ENST00000685348.1:c.*1505T>C
(RAF1)
|
ENSP00000510285.1:n.*1505T>C
|
|
|
ENST00000685437.1:c.1695T>C
(RAF1)
|
ENSP00000508794.1:p.Leu565=
|
|
|
ENST00000685653.1:c.1794T>C
(RAF1)
|
ENSP00000509968.1:p.Leu598=
|
|
|
ENST00000685697.1:n.2529T>C
(RAF1)
|
|
|
|
ENST00000685738.1:c.*758T>C
(RAF1)
|
ENSP00000510156.1:n.*758T>C
|
|
|
ENST00000686409.1:n.5203T>C
(RAF1)
|
|
|
|
ENST00000686455.1:n.4515T>C
(RAF1)
|
|
|
|
ENST00000686762.1:c.*353T>C
(RAF1)
|
ENSP00000509767.1:n.*353T>C
|
|
|
ENST00000687257.1:n.4248T>C
(RAF1)
|
|
|
|
ENST00000687326.1:c.*3086T>C
(RAF1)
|
ENSP00000509665.1:n.*3086T>C
|
|
|
ENST00000687505.1:n.1912T>C
(RAF1)
|
|
|
|
ENST00000687923.1:c.1683T>C
(RAF1)
|
ENSP00000510255.1:p.Leu561=
|
|
|
ENST00000688269.1:n.2390T>C
(RAF1)
|
|
|
|
ENST00000688444.1:n.3911T>C
(RAF1)
|
|
|
|
ENST00000688543.1:c.1695T>C
(RAF1)
|
ENSP00000509612.1:p.Leu565=
|
|
|
ENST00000688625.1:c.*3163T>C
(RAF1)
|
ENSP00000509522.1:n.*3163T>C
|
|
|
ENST00000688803.1:n.3222T>C
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1471T>C
(RAF1)
|
ENSP00000509756.1:n.*1471T>C
|
|
|
ENST00000689389.1:c.1617T>C
(RAF1)
|
ENSP00000510213.1:p.Leu539=
|
|
|
ENST00000689418.1:c.*3689T>C
(RAF1)
|
ENSP00000509467.1:n.*3689T>C
|
|
|
ENST00000689540.1:n.4162T>C
(RAF1)
|
|
|
|
ENST00000689876.1:c.*343T>C
(RAF1)
|
ENSP00000508535.1:n.*343T>C
|
|
|
ENST00000689914.1:c.*728T>C
(RAF1)
|
ENSP00000509847.1:n.*728T>C
|
|
|
ENST00000690397.1:c.1683T>C
(RAF1)
|
ENSP00000508730.1:p.Leu561=
|
|
|
ENST00000690460.1:c.1782T>C
(RAF1)
|
ENSP00000509106.1:p.Leu594=
|
|
|
ENST00000690585.1:c.520T>C
(RAF1)
|
|
|
|
ENST00000690625.1:n.2830T>C
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1666T>C
(RAF1)
|
ENSP00000510712.1:n.*1666T>C
|
|
|
ENST00000691643.1:n.2847T>C
(RAF1)
|
|
|
|
ENST00000691724.1:c.*751T>C
(RAF1)
|
ENSP00000509255.1:n.*751T>C
|
|
|
ENST00000691779.1:c.*1372T>C
(RAF1)
|
ENSP00000508592.1:n.*1372T>C
|
|
|
ENST00000691888.1:c.668T>C
(RAF1)
|
|
|
|
ENST00000691899.1:c.1794T>C
(RAF1)
|
ENSP00000508763.1:p.Leu598=
|
|
|
ENST00000692069.1:n.4718T>C
(RAF1)
|
|
|
|
ENST00000692093.1:c.1695T>C
(RAF1)
|
ENSP00000509669.1:p.Leu565=
|
|
|
ENST00000692311.1:n.2618T>C
(RAF1)
|
|
|
|
ENST00000692558.1:n.4377T>C
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1531T>C
(RAF1)
|
ENSP00000509055.1:n.*1531T>C
|
|
|
ENST00000692830.1:c.*1539T>C
(RAF1)
|
ENSP00000509461.1:n.*1539T>C
|
|
|
ENST00000693312.1:c.1569T>C
(RAF1)
|
ENSP00000508686.1:p.Leu523=
|
|
|
ENST00000693664.1:c.*245T>C
(RAF1)
|
ENSP00000509614.1:n.*245T>C
|
|
|
ENST00000693705.1:c.*1173T>C
(RAF1)
|
ENSP00000510697.1:n.*1173T>C
|
|
|
ENST00000251849.9:c.1794T>C
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Leu598=
|
|
|
ENST00000442415.7:c.1854T>C
(RAF1)
|
ENSP00000401888.2:p.Leu618=
|
|
|
ENST00000676541.1:c.*2603A>G
(MKRN2)
|
ENSP00000503730.1:n.*2603A>G
|
|
|
ENST00000677142.1:c.*2603A>G
(MKRN2)
|
ENSP00000504455.1:n.*2603A>G
|
|
|
ENST00000677816.1:c.*1158A>G
(MKRN2)
|
ENSP00000502893.1:n.*1158A>G
|
|
|
ENST00000677941.1:n.2666A>G
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1794T>C
(RAF1)
|
ENSP00000251849.4:p.Leu598=
|
|
|
ENST00000423275.5:c.*1471T>C
(RAF1)
|
ENSP00000401088.1:n.*1471T>C
|
|
|
ENST00000432427.2:c.1431T>C
(RAF1)
|
ENSP00000398591.2:p.Leu477=
|
|
|
ENST00000442415.6:c.1854T>C
(RAF1)
|
ENSP00000401888.2:p.Leu618=
|
|
|
ENST00000471449.1:n.483T>C
(RAF1)
|
|
|
|
NM_002880.3:c.1794T>C , LRG_413t1:c.1794T>C
(RAF1)
|
NP_002871.1:p.Leu598=
|
|
|
XM_005265355.1:c.1794T>C
(RAF1)
|
XP_005265412.1:p.Leu598=
|
|
|
XM_005265357.1:c.1695T>C
(RAF1)
|
XP_005265414.1:p.Leu565=
|
|
|
XM_005265358.3:c.1551T>C
(RAF1)
|
XP_005265415.1:p.Leu517=
|
|
|
XM_005265359.3:c.1452T>C
(RAF1)
|
XP_005265416.1:p.Leu484=
|
|
|
XM_011533974.1:c.1794T>C
(RAF1)
|
XP_011532276.1:p.Leu598=
|
|
|
XM_011533975.1:c.1551T>C
(RAF1)
|
XP_011532277.1:p.Leu517=
|
|
|
NM_001354689.1:c.1854T>C
(RAF1)
|
NP_001341618.1:p.Leu618=
|
|
|
NM_001354690.1:c.1794T>C
(RAF1)
|
NP_001341619.1:p.Leu598=
|
|
|
NM_001354691.1:c.1551T>C
(RAF1)
|
NP_001341620.1:p.Leu517=
|
|
|
NM_001354692.1:c.1551T>C
(RAF1)
|
NP_001341621.1:p.Leu517=
|
|
|
NM_001354693.1:c.1695T>C
(RAF1)
|
NP_001341622.1:p.Leu565=
|
|
|
NM_001354694.1:c.1611T>C
(RAF1)
|
NP_001341623.1:p.Leu537=
|
|
|
NM_001354695.1:c.1452T>C
(RAF1)
|
NP_001341624.1:p.Leu484=
|
|
|
NR_148940.1:n.2322T>C
(RAF1)
|
|
|
|
NR_148941.1:n.2268T>C
(RAF1)
|
|
|
|
NR_148942.1:n.2207T>C
(RAF1)
|
|
|
|
XM_011533974.3:c.1794T>C
(RAF1)
|
XP_011532276.1:p.Leu598=
|
|
|
XM_017006966.1:c.1695T>C
(RAF1)
|
XP_016862455.1:p.Leu565=
|
|
|
NM_001354689.3:c.1854T>C
(RAF1)
|
NP_001341618.1:p.Leu618=
|
|
|
NM_001354690.2:c.1794T>C
(RAF1)
|
NP_001341619.1:p.Leu598=
|
|
|
NM_001354691.2:c.1551T>C
(RAF1)
|
NP_001341620.1:p.Leu517=
|
|
|
NM_001354692.2:c.1551T>C
(RAF1)
|
NP_001341621.1:p.Leu517=
|
|
|
NM_001354693.2:c.1695T>C
(RAF1)
|
NP_001341622.1:p.Leu565=
|
|
|
NM_001354694.2:c.1611T>C
(RAF1)
|
NP_001341623.1:p.Leu537=
|
|
|
NM_001354695.2:c.1452T>C
(RAF1)
|
NP_001341624.1:p.Leu484=
|
|
|
NR_148940.2:n.2238T>C
(RAF1)
|
|
|
|
NR_148941.2:n.2184T>C
(RAF1)
|
|
|
|
NR_148942.2:n.2123T>C
(RAF1)
|
|
|
|
NM_001354690.3:c.1794T>C
(RAF1)
|
NP_001341619.1:p.Leu598=
|
|
|
NM_001354691.3:c.1551T>C
(RAF1)
|
NP_001341620.1:p.Leu517=
|
|
|
NM_001354692.3:c.1551T>C
(RAF1)
|
NP_001341621.1:p.Leu517=
|
|
|
NM_001354693.3:c.1695T>C
(RAF1)
|
NP_001341622.1:p.Leu565=
|
|
|
NM_001354694.3:c.1611T>C
(RAF1)
|
NP_001341623.1:p.Leu537=
|
|
|
NM_001354695.3:c.1452T>C
(RAF1)
|
NP_001341624.1:p.Leu484=
|
|
|
NM_002880.4:c.1794T>C
(RAF1)
MANE Select
|
NP_002871.1:p.Leu598=
|
|
|
NR_148940.3:n.2238T>C
(RAF1)
|
|
|
|
NR_148941.3:n.2184T>C
(RAF1)
|
|
|
|
NR_148942.3:n.2123T>C
(RAF1)
|
|
|
