|
ENST00000423275.6:c.*1603T>A
(RAF1)
|
ENSP00000401088.1:n.*1603T>A
|
|
|
ENST00000432427.3:c.1255T>A
(RAF1)
|
|
|
|
ENST00000460610.2:n.6250T>A
(RAF1)
|
|
|
|
ENST00000471449.2:n.748T>A
(RAF1)
|
|
|
|
ENST00000475353.2:n.4218T>A
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1615T>A
(RAF1)
|
ENSP00000508612.1:n.*1615T>A
|
|
|
ENST00000685348.1:c.*1649T>A
(RAF1)
|
ENSP00000510285.1:n.*1649T>A
|
|
|
ENST00000685437.1:c.1839T>A
(RAF1)
|
ENSP00000508794.1:p.Pro613=
|
|
|
ENST00000685653.1:c.1938T>A
(RAF1)
|
ENSP00000509968.1:p.Pro646=
|
|
|
ENST00000685697.1:n.2673T>A
(RAF1)
|
|
|
|
ENST00000685738.1:c.*902T>A
(RAF1)
|
ENSP00000510156.1:n.*902T>A
|
|
|
ENST00000686409.1:n.5347T>A
(RAF1)
|
|
|
|
ENST00000686455.1:n.4659T>A
(RAF1)
|
|
|
|
ENST00000686762.1:c.*497T>A
(RAF1)
|
ENSP00000509767.1:n.*497T>A
|
|
|
ENST00000687257.1:n.4392T>A
(RAF1)
|
|
|
|
ENST00000687326.1:c.*3230T>A
(RAF1)
|
ENSP00000509665.1:n.*3230T>A
|
|
|
ENST00000687505.1:n.2056T>A
(RAF1)
|
|
|
|
ENST00000687923.1:c.1827T>A
(RAF1)
|
ENSP00000510255.1:p.Pro609=
|
|
|
ENST00000688269.1:n.2534T>A
(RAF1)
|
|
|
|
ENST00000688444.1:n.4055T>A
(RAF1)
|
|
|
|
ENST00000688543.1:c.1839T>A
(RAF1)
|
ENSP00000509612.1:p.Pro613=
|
|
|
ENST00000688625.1:c.*3307T>A
(RAF1)
|
ENSP00000509522.1:n.*3307T>A
|
|
|
ENST00000688803.1:n.3366T>A
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1615T>A
(RAF1)
|
ENSP00000509756.1:n.*1615T>A
|
|
|
ENST00000689389.1:c.1761T>A
(RAF1)
|
ENSP00000510213.1:p.Pro587=
|
|
|
ENST00000689418.1:c.*3833T>A
(RAF1)
|
ENSP00000509467.1:n.*3833T>A
|
|
|
ENST00000689540.1:n.4306T>A
(RAF1)
|
|
|
|
ENST00000689876.1:c.*487T>A
(RAF1)
|
ENSP00000508535.1:n.*487T>A
|
|
|
ENST00000689914.1:c.*872T>A
(RAF1)
|
ENSP00000509847.1:n.*872T>A
|
|
|
ENST00000690397.1:c.1827T>A
(RAF1)
|
ENSP00000508730.1:p.Pro609=
|
|
|
ENST00000690460.1:c.1926T>A
(RAF1)
|
ENSP00000509106.1:p.Pro642=
|
|
|
ENST00000690585.1:c.664T>A
(RAF1)
|
|
|
|
ENST00000690625.1:n.2974T>A
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1810T>A
(RAF1)
|
ENSP00000510712.1:n.*1810T>A
|
|
|
ENST00000691643.1:n.2991T>A
(RAF1)
|
|
|
|
ENST00000691724.1:c.*895T>A
(RAF1)
|
ENSP00000509255.1:n.*895T>A
|
|
|
ENST00000691779.1:c.*1516T>A
(RAF1)
|
ENSP00000508592.1:n.*1516T>A
|
|
|
ENST00000691888.1:c.812T>A
(RAF1)
|
|
|
|
ENST00000691899.1:c.1938T>A
(RAF1)
|
ENSP00000508763.1:p.Pro646=
|
|
|
ENST00000692069.1:n.4862T>A
(RAF1)
|
|
|
|
ENST00000692093.1:c.1839T>A
(RAF1)
|
ENSP00000509669.1:p.Pro613=
|
|
|
ENST00000692311.1:n.2762T>A
(RAF1)
|
|
|
|
ENST00000692558.1:n.4521T>A
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1675T>A
(RAF1)
|
ENSP00000509055.1:n.*1675T>A
|
|
|
ENST00000692830.1:c.*1683T>A
(RAF1)
|
ENSP00000509461.1:n.*1683T>A
|
|
|
ENST00000693312.1:c.1713T>A
(RAF1)
|
ENSP00000508686.1:p.Pro571=
|
|
|
ENST00000693664.1:c.*389T>A
(RAF1)
|
ENSP00000509614.1:n.*389T>A
|
|
|
ENST00000693705.1:c.*1317T>A
(RAF1)
|
ENSP00000510697.1:n.*1317T>A
|
|
|
ENST00000251849.9:c.1938T>A
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Pro646=
|
|
|
ENST00000442415.7:c.1998T>A
(RAF1)
|
ENSP00000401888.2:p.Pro666=
|
|
|
ENST00000676541.1:c.*2270A>T
(MKRN2)
|
ENSP00000503730.1:n.*2270A>T
|
|
|
ENST00000677142.1:c.*2270A>T
(MKRN2)
|
ENSP00000504455.1:n.*2270A>T
|
|
|
ENST00000677816.1:c.*825A>T
(MKRN2)
|
ENSP00000502893.1:n.*825A>T
|
|
|
ENST00000677941.1:n.2333A>T
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1938T>A
(RAF1)
|
ENSP00000251849.4:p.Pro646=
|
|
|
ENST00000423275.5:c.*1615T>A
(RAF1)
|
ENSP00000401088.1:n.*1615T>A
|
|
|
ENST00000432427.2:c.1575T>A
(RAF1)
|
ENSP00000398591.2:p.Pro525=
|
|
|
ENST00000442415.6:c.1998T>A
(RAF1)
|
ENSP00000401888.2:p.Pro666=
|
|
|
ENST00000471449.1:n.627T>A
(RAF1)
|
|
|
|
NM_002880.3:c.1938T>A , LRG_413t1:c.1938T>A
(RAF1)
|
NP_002871.1:p.Pro646=
|
|
|
XM_005265355.1:c.1938T>A
(RAF1)
|
XP_005265412.1:p.Pro646=
|
|
|
XM_005265357.1:c.1839T>A
(RAF1)
|
XP_005265414.1:p.Pro613=
|
|
|
XM_005265358.3:c.1695T>A
(RAF1)
|
XP_005265415.1:p.Pro565=
|
|
|
XM_005265359.3:c.1596T>A
(RAF1)
|
XP_005265416.1:p.Pro532=
|
|
|
XM_011533974.1:c.1938T>A
(RAF1)
|
XP_011532276.1:p.Pro646=
|
|
|
XM_011533975.1:c.1695T>A
(RAF1)
|
XP_011532277.1:p.Pro565=
|
|
|
NM_001354689.1:c.1998T>A
(RAF1)
|
NP_001341618.1:p.Pro666=
|
|
|
NM_001354690.1:c.1938T>A
(RAF1)
|
NP_001341619.1:p.Pro646=
|
|
|
NM_001354691.1:c.1695T>A
(RAF1)
|
NP_001341620.1:p.Pro565=
|
|
|
NM_001354692.1:c.1695T>A
(RAF1)
|
NP_001341621.1:p.Pro565=
|
|
|
NM_001354693.1:c.1839T>A
(RAF1)
|
NP_001341622.1:p.Pro613=
|
|
|
NM_001354694.1:c.1755T>A
(RAF1)
|
NP_001341623.1:p.Pro585=
|
|
|
NM_001354695.1:c.1596T>A
(RAF1)
|
NP_001341624.1:p.Pro532=
|
|
|
NR_148940.1:n.2466T>A
(RAF1)
|
|
|
|
NR_148941.1:n.2412T>A
(RAF1)
|
|
|
|
NR_148942.1:n.2351T>A
(RAF1)
|
|
|
|
XM_011533974.3:c.1938T>A
(RAF1)
|
XP_011532276.1:p.Pro646=
|
|
|
XM_017006966.1:c.1839T>A
(RAF1)
|
XP_016862455.1:p.Pro613=
|
|
|
NM_001354689.3:c.1998T>A
(RAF1)
|
NP_001341618.1:p.Pro666=
|
|
|
NM_001354690.2:c.1938T>A
(RAF1)
|
NP_001341619.1:p.Pro646=
|
|
|
NM_001354691.2:c.1695T>A
(RAF1)
|
NP_001341620.1:p.Pro565=
|
|
|
NM_001354692.2:c.1695T>A
(RAF1)
|
NP_001341621.1:p.Pro565=
|
|
|
NM_001354693.2:c.1839T>A
(RAF1)
|
NP_001341622.1:p.Pro613=
|
|
|
NM_001354694.2:c.1755T>A
(RAF1)
|
NP_001341623.1:p.Pro585=
|
|
|
NM_001354695.2:c.1596T>A
(RAF1)
|
NP_001341624.1:p.Pro532=
|
|
|
NR_148940.2:n.2382T>A
(RAF1)
|
|
|
|
NR_148941.2:n.2328T>A
(RAF1)
|
|
|
|
NR_148942.2:n.2267T>A
(RAF1)
|
|
|
|
NM_001354690.3:c.1938T>A
(RAF1)
|
NP_001341619.1:p.Pro646=
|
|
|
NM_001354691.3:c.1695T>A
(RAF1)
|
NP_001341620.1:p.Pro565=
|
|
|
NM_001354692.3:c.1695T>A
(RAF1)
|
NP_001341621.1:p.Pro565=
|
|
|
NM_001354693.3:c.1839T>A
(RAF1)
|
NP_001341622.1:p.Pro613=
|
|
|
NM_001354694.3:c.1755T>A
(RAF1)
|
NP_001341623.1:p.Pro585=
|
|
|
NM_001354695.3:c.1596T>A
(RAF1)
|
NP_001341624.1:p.Pro532=
|
|
|
NM_002880.4:c.1938T>A
(RAF1)
MANE Select
|
NP_002871.1:p.Pro646=
|
|
|
NR_148940.3:n.2382T>A
(RAF1)
|
|
|
|
NR_148941.3:n.2328T>A
(RAF1)
|
|
|
|
NR_148942.3:n.2267T>A
(RAF1)
|
|
|
