|
ENST00000423275.6:c.*1201+56G>T
(RAF1)
|
ENSP00000401088.1:n.*1201+56G>T
|
|
|
ENST00000432427.3:c.853+56G>T
(RAF1)
|
|
|
|
ENST00000460610.2:n.5337G>T
(RAF1)
|
|
|
|
ENST00000471449.2:n.346+56G>T
(RAF1)
|
|
|
|
ENST00000475353.2:n.3305G>T
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1213+56G>T
(RAF1)
|
ENSP00000508612.1:n.*1213+56G>T
|
|
|
ENST00000685348.1:c.*1095-219G>T
(RAF1)
|
ENSP00000510285.1:n.*1095-219G>T
|
|
|
ENST00000685437.1:c.1437+56G>T
(RAF1)
|
ENSP00000508794.1:n.1437+56G>T
|
|
|
ENST00000685653.1:c.1536+56G>T
(RAF1)
|
ENSP00000509968.1:n.1536+56G>T
|
|
|
ENST00000685697.1:n.2271+56G>T
(RAF1)
|
|
|
|
ENST00000685738.1:c.*500+56G>T
(RAF1)
|
ENSP00000510156.1:n.*500+56G>T
|
|
|
ENST00000686409.1:n.4434G>T
(RAF1)
|
|
|
|
ENST00000686455.1:n.3746G>T
(RAF1)
|
|
|
|
ENST00000686762.1:c.*95+56G>T
(RAF1)
|
ENSP00000509767.1:n.*95+56G>T
|
|
|
ENST00000687257.1:n.3619G>T
(RAF1)
|
|
|
|
ENST00000687326.1:c.*2317G>T
(RAF1)
|
ENSP00000509665.1:n.*2317G>T
|
|
|
ENST00000687505.1:n.1654+56G>T
(RAF1)
|
|
|
|
ENST00000687923.1:c.1425+56G>T
(RAF1)
|
ENSP00000510255.1:n.1425+56G>T
|
|
|
ENST00000688269.1:n.2132+56G>T
(RAF1)
|
|
|
|
ENST00000688444.1:n.3653+56G>T
(RAF1)
|
|
|
|
ENST00000688543.1:c.1437+56G>T
(RAF1)
|
ENSP00000509612.1:n.1437+56G>T
|
|
|
ENST00000688625.1:c.*2905+56G>T
(RAF1)
|
ENSP00000509522.1:n.*2905+56G>T
|
|
|
ENST00000688803.1:n.2965-372G>T
(RAF1)
|
|
|
|
ENST00000688914.1:n.578G>T
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1213+56G>T
(RAF1)
|
ENSP00000509756.1:n.*1213+56G>T
|
|
|
ENST00000689389.1:c.1359+56G>T
(RAF1)
|
ENSP00000510213.1:n.1359+56G>T
|
|
|
ENST00000689418.1:c.*3060G>T
(RAF1)
|
ENSP00000509467.1:n.*3060G>T
|
|
|
ENST00000689540.1:n.3533G>T
(RAF1)
|
|
|
|
ENST00000689876.1:c.1418-219G>T
(RAF1)
|
ENSP00000508535.1:n.1418-219G>T
|
|
|
ENST00000689914.1:c.*470+56G>T
(RAF1)
|
ENSP00000509847.1:n.*470+56G>T
|
|
|
ENST00000690397.1:c.1425+56G>T
(RAF1)
|
ENSP00000508730.1:n.1425+56G>T
|
|
|
ENST00000690460.1:c.1524+56G>T
(RAF1)
|
ENSP00000509106.1:n.1524+56G>T
|
|
|
ENST00000690585.1:c.263-372G>T
(RAF1)
|
|
|
|
ENST00000690625.1:n.2572+56G>T
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1408+56G>T
(RAF1)
|
ENSP00000510712.1:n.*1408+56G>T
|
|
|
ENST00000691643.1:n.2218G>T
(RAF1)
|
|
|
|
ENST00000691724.1:c.*493+56G>T
(RAF1)
|
ENSP00000509255.1:n.*493+56G>T
|
|
|
ENST00000691779.1:c.*1114+56G>T
(RAF1)
|
ENSP00000508592.1:n.*1114+56G>T
|
|
|
ENST00000691888.1:c.410+56G>T
(RAF1)
|
|
|
|
ENST00000691899.1:c.1536+56G>T
(RAF1)
|
ENSP00000508763.1:n.1536+56G>T
|
|
|
ENST00000692069.1:n.3949G>T
(RAF1)
|
|
|
|
ENST00000692093.1:c.1437+56G>T
(RAF1)
|
ENSP00000509669.1:n.1437+56G>T
|
|
|
ENST00000692311.1:n.2360+56G>T
(RAF1)
|
|
|
|
ENST00000692558.1:n.3748G>T
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1273+56G>T
(RAF1)
|
ENSP00000509055.1:n.*1273+56G>T
|
|
|
ENST00000692830.1:c.*1281+56G>T
(RAF1)
|
ENSP00000509461.1:n.*1281+56G>T
|
|
|
ENST00000693312.1:c.1311+56G>T
(RAF1)
|
ENSP00000508686.1:n.1311+56G>T
|
|
|
ENST00000693664.1:c.1488-372G>T
(RAF1)
|
ENSP00000509614.1:n.1488-372G>T
|
|
|
ENST00000693705.1:c.*1048-644G>T
(RAF1)
|
ENSP00000510697.1:n.*1048-644G>T
|
|
|
ENST00000251849.9:c.1536+56G>T
(RAF1)
MANE Select
|
ENSP00000251849.4:n.1536+56G>T
|
|
|
ENST00000442415.7:c.1596+56G>T
(RAF1)
|
ENSP00000401888.2:n.1596+56G>T
|
|
|
ENST00000676541.1:c.*3372C>A
(MKRN2)
|
ENSP00000503730.1:n.*3372C>A
|
|
|
ENST00000677142.1:c.*3372C>A
(MKRN2)
|
ENSP00000504455.1:n.*3372C>A
|
|
|
ENST00000677816.1:c.*1927C>A
(MKRN2)
|
ENSP00000502893.1:n.*1927C>A
|
|
|
ENST00000677941.1:n.3435C>A
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1536+56G>T
(RAF1)
|
ENSP00000251849.4:n.1536+56G>T
|
|
|
ENST00000423275.5:c.*1213+56G>T
(RAF1)
|
ENSP00000401088.1:n.*1213+56G>T
|
|
|
ENST00000432427.2:c.1173+56G>T
(RAF1)
|
ENSP00000398591.2:n.1173+56G>T
|
|
|
ENST00000442415.6:c.1596+56G>T
(RAF1)
|
ENSP00000401888.2:n.1596+56G>T
|
|
|
ENST00000471449.1:n.225+56G>T
(RAF1)
|
|
|
|
NM_002880.3:c.1536+56G>T , LRG_413t1:c.1536+56G>T
(RAF1)
|
NP_002871.1:n.1536+56G>T
|
|
|
XM_005265355.1:c.1536+56G>T
(RAF1)
|
XP_005265412.1:n.1536+56G>T
|
|
|
XM_005265357.1:c.1437+56G>T
(RAF1)
|
XP_005265414.1:n.1437+56G>T
|
|
|
XM_005265358.3:c.1293+56G>T
(RAF1)
|
XP_005265415.1:n.1293+56G>T
|
|
|
XM_005265359.3:c.1194+56G>T
(RAF1)
|
XP_005265416.1:n.1194+56G>T
|
|
|
XM_005265360.1:c.1418-219G>T
(RAF1)
|
XP_005265417.1:n.1418-219G>T
|
|
|
XM_011533974.1:c.1536+56G>T
(RAF1)
|
XP_011532276.1:n.1536+56G>T
|
|
|
XM_011533975.1:c.1293+56G>T
(RAF1)
|
XP_011532277.1:n.1293+56G>T
|
|
|
NM_001354689.1:c.1596+56G>T
(RAF1)
|
NP_001341618.1:n.1596+56G>T
|
|
|
NM_001354690.1:c.1536+56G>T
(RAF1)
|
NP_001341619.1:n.1536+56G>T
|
|
|
NM_001354691.1:c.1293+56G>T
(RAF1)
|
NP_001341620.1:n.1293+56G>T
|
|
|
NM_001354692.1:c.1293+56G>T
(RAF1)
|
NP_001341621.1:n.1293+56G>T
|
|
|
NM_001354693.1:c.1437+56G>T
(RAF1)
|
NP_001341622.1:n.1437+56G>T
|
|
|
NM_001354694.1:c.1353+56G>T
(RAF1)
|
NP_001341623.1:n.1353+56G>T
|
|
|
NM_001354695.1:c.1194+56G>T
(RAF1)
|
NP_001341624.1:n.1194+56G>T
|
|
|
NR_148940.1:n.2064+56G>T
(RAF1)
|
|
|
|
NR_148941.1:n.2010+56G>T
(RAF1)
|
|
|
|
NR_148942.1:n.1949+56G>T
(RAF1)
|
|
|
|
XM_011533974.3:c.1536+56G>T
(RAF1)
|
XP_011532276.1:n.1536+56G>T
|
|
|
XM_017006966.1:c.1437+56G>T
(RAF1)
|
XP_016862455.1:n.1437+56G>T
|
|
|
NM_001354689.3:c.1596+56G>T
(RAF1)
|
NP_001341618.1:n.1596+56G>T
|
|
|
NM_001354690.2:c.1536+56G>T
(RAF1)
|
NP_001341619.1:n.1536+56G>T
|
|
|
NM_001354691.2:c.1293+56G>T
(RAF1)
|
NP_001341620.1:n.1293+56G>T
|
|
|
NM_001354692.2:c.1293+56G>T
(RAF1)
|
NP_001341621.1:n.1293+56G>T
|
|
|
NM_001354693.2:c.1437+56G>T
(RAF1)
|
NP_001341622.1:n.1437+56G>T
|
|
|
NM_001354694.2:c.1353+56G>T
(RAF1)
|
NP_001341623.1:n.1353+56G>T
|
|
|
NM_001354695.2:c.1194+56G>T
(RAF1)
|
NP_001341624.1:n.1194+56G>T
|
|
|
NR_148940.2:n.1980+56G>T
(RAF1)
|
|
|
|
NR_148941.2:n.1926+56G>T
(RAF1)
|
|
|
|
NR_148942.2:n.1865+56G>T
(RAF1)
|
|
|
|
NM_001354690.3:c.1536+56G>T
(RAF1)
|
NP_001341619.1:n.1536+56G>T
|
|
|
NM_001354691.3:c.1293+56G>T
(RAF1)
|
NP_001341620.1:n.1293+56G>T
|
|
|
NM_001354692.3:c.1293+56G>T
(RAF1)
|
NP_001341621.1:n.1293+56G>T
|
|
|
NM_001354693.3:c.1437+56G>T
(RAF1)
|
NP_001341622.1:n.1437+56G>T
|
|
|
NM_001354694.3:c.1353+56G>T
(RAF1)
|
NP_001341623.1:n.1353+56G>T
|
|
|
NM_001354695.3:c.1194+56G>T
(RAF1)
|
NP_001341624.1:n.1194+56G>T
|
|
|
NM_002880.4:c.1536+56G>T
(RAF1)
MANE Select
|
NP_002871.1:n.1536+56G>T
|
|
|
NR_148940.3:n.1980+56G>T
(RAF1)
|
|
|
|
NR_148941.3:n.1926+56G>T
(RAF1)
|
|
|
|
NR_148942.3:n.1865+56G>T
(RAF1)
|
|
|
