|
ENST00000423275.6:c.*1252G>A
(RAF1)
|
ENSP00000401088.1:n.*1252G>A
|
|
|
ENST00000432427.3:c.904G>A
(RAF1)
|
|
|
|
ENST00000460610.2:n.5759G>A
(RAF1)
|
|
|
|
ENST00000471449.2:n.397G>A
(RAF1)
|
|
|
|
ENST00000475353.2:n.3727G>A
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1264G>A
(RAF1)
|
ENSP00000508612.1:n.*1264G>A
|
|
|
ENST00000685348.1:c.*1298G>A
(RAF1)
|
ENSP00000510285.1:n.*1298G>A
|
|
|
ENST00000685437.1:c.1488G>A
(RAF1)
|
ENSP00000508794.1:p.Ser496=
|
|
|
ENST00000685653.1:c.1587G>A
(RAF1)
|
ENSP00000509968.1:p.Ser529=
|
|
|
ENST00000685697.1:n.2322G>A
(RAF1)
|
|
|
|
ENST00000685738.1:c.*551G>A
(RAF1)
|
ENSP00000510156.1:n.*551G>A
|
|
|
ENST00000686409.1:n.4856G>A
(RAF1)
|
|
|
|
ENST00000686455.1:n.4168G>A
(RAF1)
|
|
|
|
ENST00000686762.1:c.*146G>A
(RAF1)
|
ENSP00000509767.1:n.*146G>A
|
|
|
ENST00000687257.1:n.4041G>A
(RAF1)
|
|
|
|
ENST00000687326.1:c.*2739G>A
(RAF1)
|
ENSP00000509665.1:n.*2739G>A
|
|
|
ENST00000687505.1:n.1705G>A
(RAF1)
|
|
|
|
ENST00000687923.1:c.1476G>A
(RAF1)
|
ENSP00000510255.1:p.Ser492=
|
|
|
ENST00000688269.1:n.2183G>A
(RAF1)
|
|
|
|
ENST00000688444.1:n.3704G>A
(RAF1)
|
|
|
|
ENST00000688543.1:c.1488G>A
(RAF1)
|
ENSP00000509612.1:p.Ser496=
|
|
|
ENST00000688625.1:c.*2956G>A
(RAF1)
|
ENSP00000509522.1:n.*2956G>A
|
|
|
ENST00000688803.1:n.3015G>A
(RAF1)
|
|
|
|
ENST00000688914.1:n.1000G>A
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1264G>A
(RAF1)
|
ENSP00000509756.1:n.*1264G>A
|
|
|
ENST00000689389.1:c.1410G>A
(RAF1)
|
ENSP00000510213.1:p.Ser470=
|
|
|
ENST00000689418.1:c.*3482G>A
(RAF1)
|
ENSP00000509467.1:n.*3482G>A
|
|
|
ENST00000689540.1:n.3955G>A
(RAF1)
|
|
|
|
ENST00000689876.1:c.*136G>A
(RAF1)
|
ENSP00000508535.1:n.*136G>A
|
|
|
ENST00000689914.1:c.*521G>A
(RAF1)
|
ENSP00000509847.1:n.*521G>A
|
|
|
ENST00000690397.1:c.1476G>A
(RAF1)
|
ENSP00000508730.1:p.Ser492=
|
|
|
ENST00000690460.1:c.1575G>A
(RAF1)
|
ENSP00000509106.1:p.Ser525=
|
|
|
ENST00000690585.1:c.313G>A
(RAF1)
|
|
|
|
ENST00000690625.1:n.2623G>A
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1459G>A
(RAF1)
|
ENSP00000510712.1:n.*1459G>A
|
|
|
ENST00000691643.1:n.2640G>A
(RAF1)
|
|
|
|
ENST00000691724.1:c.*544G>A
(RAF1)
|
ENSP00000509255.1:n.*544G>A
|
|
|
ENST00000691779.1:c.*1165G>A
(RAF1)
|
ENSP00000508592.1:n.*1165G>A
|
|
|
ENST00000691888.1:c.461G>A
(RAF1)
|
|
|
|
ENST00000691899.1:c.1587G>A
(RAF1)
|
ENSP00000508763.1:p.Ser529=
|
|
|
ENST00000692069.1:n.4371G>A
(RAF1)
|
|
|
|
ENST00000692093.1:c.1488G>A
(RAF1)
|
ENSP00000509669.1:p.Ser496=
|
|
|
ENST00000692311.1:n.2411G>A
(RAF1)
|
|
|
|
ENST00000692558.1:n.4170G>A
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1324G>A
(RAF1)
|
ENSP00000509055.1:n.*1324G>A
|
|
|
ENST00000692830.1:c.*1332G>A
(RAF1)
|
ENSP00000509461.1:n.*1332G>A
|
|
|
ENST00000693312.1:c.1362G>A
(RAF1)
|
ENSP00000508686.1:p.Ser454=
|
|
|
ENST00000693664.1:c.*38G>A
(RAF1)
|
ENSP00000509614.1:n.*38G>A
|
|
|
ENST00000693705.1:c.*1048-222G>A
(RAF1)
|
ENSP00000510697.1:n.*1048-222G>A
|
|
|
ENST00000251849.9:c.1587G>A
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Ser529=
|
|
|
ENST00000442415.7:c.1647G>A
(RAF1)
|
ENSP00000401888.2:p.Ser549=
|
|
|
ENST00000676541.1:c.*2950C>T
(MKRN2)
|
ENSP00000503730.1:n.*2950C>T
|
|
|
ENST00000677142.1:c.*2950C>T
(MKRN2)
|
ENSP00000504455.1:n.*2950C>T
|
|
|
ENST00000677816.1:c.*1505C>T
(MKRN2)
|
ENSP00000502893.1:n.*1505C>T
|
|
|
ENST00000677941.1:n.3013C>T
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1587G>A
(RAF1)
|
ENSP00000251849.4:p.Ser529=
|
|
|
ENST00000423275.5:c.*1264G>A
(RAF1)
|
ENSP00000401088.1:n.*1264G>A
|
|
|
ENST00000432427.2:c.1224G>A
(RAF1)
|
ENSP00000398591.2:p.Ser408=
|
|
|
ENST00000442415.6:c.1647G>A
(RAF1)
|
ENSP00000401888.2:p.Ser549=
|
|
|
ENST00000471449.1:n.276G>A
(RAF1)
|
|
|
|
NM_002880.3:c.1587G>A , LRG_413t1:c.1587G>A
(RAF1)
|
NP_002871.1:p.Ser529=
|
|
|
XM_005265355.1:c.1587G>A
(RAF1)
|
XP_005265412.1:p.Ser529=
|
|
|
XM_005265357.1:c.1488G>A
(RAF1)
|
XP_005265414.1:p.Ser496=
|
|
|
XM_005265358.3:c.1344G>A
(RAF1)
|
XP_005265415.1:p.Ser448=
|
|
|
XM_005265359.3:c.1245G>A
(RAF1)
|
XP_005265416.1:p.Ser415=
|
|
|
XM_011533974.1:c.1587G>A
(RAF1)
|
XP_011532276.1:p.Ser529=
|
|
|
XM_011533975.1:c.1344G>A
(RAF1)
|
XP_011532277.1:p.Ser448=
|
|
|
NM_001354689.1:c.1647G>A
(RAF1)
|
NP_001341618.1:p.Ser549=
|
|
|
NM_001354690.1:c.1587G>A
(RAF1)
|
NP_001341619.1:p.Ser529=
|
|
|
NM_001354691.1:c.1344G>A
(RAF1)
|
NP_001341620.1:p.Ser448=
|
|
|
NM_001354692.1:c.1344G>A
(RAF1)
|
NP_001341621.1:p.Ser448=
|
|
|
NM_001354693.1:c.1488G>A
(RAF1)
|
NP_001341622.1:p.Ser496=
|
|
|
NM_001354694.1:c.1404G>A
(RAF1)
|
NP_001341623.1:p.Ser468=
|
|
|
NM_001354695.1:c.1245G>A
(RAF1)
|
NP_001341624.1:p.Ser415=
|
|
|
NR_148940.1:n.2115G>A
(RAF1)
|
|
|
|
NR_148941.1:n.2061G>A
(RAF1)
|
|
|
|
NR_148942.1:n.2000G>A
(RAF1)
|
|
|
|
XM_011533974.3:c.1587G>A
(RAF1)
|
XP_011532276.1:p.Ser529=
|
|
|
XM_017006966.1:c.1488G>A
(RAF1)
|
XP_016862455.1:p.Ser496=
|
|
|
NM_001354689.3:c.1647G>A
(RAF1)
|
NP_001341618.1:p.Ser549=
|
|
|
NM_001354690.2:c.1587G>A
(RAF1)
|
NP_001341619.1:p.Ser529=
|
|
|
NM_001354691.2:c.1344G>A
(RAF1)
|
NP_001341620.1:p.Ser448=
|
|
|
NM_001354692.2:c.1344G>A
(RAF1)
|
NP_001341621.1:p.Ser448=
|
|
|
NM_001354693.2:c.1488G>A
(RAF1)
|
NP_001341622.1:p.Ser496=
|
|
|
NM_001354694.2:c.1404G>A
(RAF1)
|
NP_001341623.1:p.Ser468=
|
|
|
NM_001354695.2:c.1245G>A
(RAF1)
|
NP_001341624.1:p.Ser415=
|
|
|
NR_148940.2:n.2031G>A
(RAF1)
|
|
|
|
NR_148941.2:n.1977G>A
(RAF1)
|
|
|
|
NR_148942.2:n.1916G>A
(RAF1)
|
|
|
|
NM_001354690.3:c.1587G>A
(RAF1)
|
NP_001341619.1:p.Ser529=
|
|
|
NM_001354691.3:c.1344G>A
(RAF1)
|
NP_001341620.1:p.Ser448=
|
|
|
NM_001354692.3:c.1344G>A
(RAF1)
|
NP_001341621.1:p.Ser448=
|
|
|
NM_001354693.3:c.1488G>A
(RAF1)
|
NP_001341622.1:p.Ser496=
|
|
|
NM_001354694.3:c.1404G>A
(RAF1)
|
NP_001341623.1:p.Ser468=
|
|
|
NM_001354695.3:c.1245G>A
(RAF1)
|
NP_001341624.1:p.Ser415=
|
|
|
NM_002880.4:c.1587G>A
(RAF1)
MANE Select
|
NP_002871.1:p.Ser529=
|
|
|
NR_148940.3:n.2031G>A
(RAF1)
|
|
|
|
NR_148941.3:n.1977G>A
(RAF1)
|
|
|
|
NR_148942.3:n.1916G>A
(RAF1)
|
|
|
