|
ENST00000423275.6:c.*1458T>A
(RAF1)
|
ENSP00000401088.1:n.*1458T>A
|
|
|
ENST00000432427.3:c.1110T>A
(RAF1)
|
|
|
|
ENST00000460610.2:n.6105T>A
(RAF1)
|
|
|
|
ENST00000471449.2:n.603T>A
(RAF1)
|
|
|
|
ENST00000475353.2:n.4073T>A
(RAF1)
|
|
|
|
ENST00000684903.1:c.*1470T>A
(RAF1)
|
ENSP00000508612.1:n.*1470T>A
|
|
|
ENST00000685348.1:c.*1504T>A
(RAF1)
|
ENSP00000510285.1:n.*1504T>A
|
|
|
ENST00000685437.1:c.1694T>A
(RAF1)
|
ENSP00000508794.1:p.Leu565His
|
|
|
ENST00000685653.1:c.1793T>A
(RAF1)
|
ENSP00000509968.1:p.Leu598His
|
|
|
ENST00000685697.1:n.2528T>A
(RAF1)
|
|
|
|
ENST00000685738.1:c.*757T>A
(RAF1)
|
ENSP00000510156.1:n.*757T>A
|
|
|
ENST00000686409.1:n.5202T>A
(RAF1)
|
|
|
|
ENST00000686455.1:n.4514T>A
(RAF1)
|
|
|
|
ENST00000686762.1:c.*352T>A
(RAF1)
|
ENSP00000509767.1:n.*352T>A
|
|
|
ENST00000687257.1:n.4247T>A
(RAF1)
|
|
|
|
ENST00000687326.1:c.*3085T>A
(RAF1)
|
ENSP00000509665.1:n.*3085T>A
|
|
|
ENST00000687505.1:n.1911T>A
(RAF1)
|
|
|
|
ENST00000687923.1:c.1682T>A
(RAF1)
|
ENSP00000510255.1:p.Leu561His
|
|
|
ENST00000688269.1:n.2389T>A
(RAF1)
|
|
|
|
ENST00000688444.1:n.3910T>A
(RAF1)
|
|
|
|
ENST00000688543.1:c.1694T>A
(RAF1)
|
ENSP00000509612.1:p.Leu565His
|
|
|
ENST00000688625.1:c.*3162T>A
(RAF1)
|
ENSP00000509522.1:n.*3162T>A
|
|
|
ENST00000688803.1:n.3221T>A
(RAF1)
|
|
|
|
ENST00000689097.1:c.*1470T>A
(RAF1)
|
ENSP00000509756.1:n.*1470T>A
|
|
|
ENST00000689389.1:c.1616T>A
(RAF1)
|
ENSP00000510213.1:p.Leu539His
|
|
|
ENST00000689418.1:c.*3688T>A
(RAF1)
|
ENSP00000509467.1:n.*3688T>A
|
|
|
ENST00000689540.1:n.4161T>A
(RAF1)
|
|
|
|
ENST00000689876.1:c.*342T>A
(RAF1)
|
ENSP00000508535.1:n.*342T>A
|
|
|
ENST00000689914.1:c.*727T>A
(RAF1)
|
ENSP00000509847.1:n.*727T>A
|
|
|
ENST00000690397.1:c.1682T>A
(RAF1)
|
ENSP00000508730.1:p.Leu561His
|
|
|
ENST00000690460.1:c.1781T>A
(RAF1)
|
ENSP00000509106.1:p.Leu594His
|
|
|
ENST00000690585.1:c.519T>A
(RAF1)
|
|
|
|
ENST00000690625.1:n.2829T>A
(RAF1)
|
|
|
|
ENST00000691396.1:c.*1665T>A
(RAF1)
|
ENSP00000510712.1:n.*1665T>A
|
|
|
ENST00000691643.1:n.2846T>A
(RAF1)
|
|
|
|
ENST00000691724.1:c.*750T>A
(RAF1)
|
ENSP00000509255.1:n.*750T>A
|
|
|
ENST00000691779.1:c.*1371T>A
(RAF1)
|
ENSP00000508592.1:n.*1371T>A
|
|
|
ENST00000691888.1:c.667T>A
(RAF1)
|
|
|
|
ENST00000691899.1:c.1793T>A
(RAF1)
|
ENSP00000508763.1:p.Leu598His
|
|
|
ENST00000692069.1:n.4717T>A
(RAF1)
|
|
|
|
ENST00000692093.1:c.1694T>A
(RAF1)
|
ENSP00000509669.1:p.Leu565His
|
|
|
ENST00000692311.1:n.2617T>A
(RAF1)
|
|
|
|
ENST00000692558.1:n.4376T>A
(RAF1)
|
|
|
|
ENST00000692773.1:c.*1530T>A
(RAF1)
|
ENSP00000509055.1:n.*1530T>A
|
|
|
ENST00000692830.1:c.*1538T>A
(RAF1)
|
ENSP00000509461.1:n.*1538T>A
|
|
|
ENST00000693312.1:c.1568T>A
(RAF1)
|
ENSP00000508686.1:p.Leu523His
|
|
|
ENST00000693664.1:c.*244T>A
(RAF1)
|
ENSP00000509614.1:n.*244T>A
|
|
|
ENST00000693705.1:c.*1172T>A
(RAF1)
|
ENSP00000510697.1:n.*1172T>A
|
|
|
ENST00000251849.9:c.1793T>A
(RAF1)
MANE Select
|
ENSP00000251849.4:p.Leu598His
|
|
|
ENST00000442415.7:c.1853T>A
(RAF1)
|
ENSP00000401888.2:p.Leu618His
|
|
|
ENST00000676541.1:c.*2604A>T
(MKRN2)
|
ENSP00000503730.1:n.*2604A>T
|
|
|
ENST00000677142.1:c.*2604A>T
(MKRN2)
|
ENSP00000504455.1:n.*2604A>T
|
|
|
ENST00000677816.1:c.*1159A>T
(MKRN2)
|
ENSP00000502893.1:n.*1159A>T
|
|
|
ENST00000677941.1:n.2667A>T
(MKRN2)
|
|
|
|
ENST00000251849.8:c.1793T>A
(RAF1)
|
ENSP00000251849.4:p.Leu598His
|
|
|
ENST00000423275.5:c.*1470T>A
(RAF1)
|
ENSP00000401088.1:n.*1470T>A
|
|
|
ENST00000432427.2:c.1430T>A
(RAF1)
|
ENSP00000398591.2:p.Leu477His
|
|
|
ENST00000442415.6:c.1853T>A
(RAF1)
|
ENSP00000401888.2:p.Leu618His
|
|
|
ENST00000471449.1:n.482T>A
(RAF1)
|
|
|
|
NM_002880.3:c.1793T>A , LRG_413t1:c.1793T>A
(RAF1)
|
NP_002871.1:p.Leu598His
|
|
|
XM_005265355.1:c.1793T>A
(RAF1)
|
XP_005265412.1:p.Leu598His
|
|
|
XM_005265357.1:c.1694T>A
(RAF1)
|
XP_005265414.1:p.Leu565His
|
|
|
XM_005265358.3:c.1550T>A
(RAF1)
|
XP_005265415.1:p.Leu517His
|
|
|
XM_005265359.3:c.1451T>A
(RAF1)
|
XP_005265416.1:p.Leu484His
|
|
|
XM_011533974.1:c.1793T>A
(RAF1)
|
XP_011532276.1:p.Leu598His
|
|
|
XM_011533975.1:c.1550T>A
(RAF1)
|
XP_011532277.1:p.Leu517His
|
|
|
NM_001354689.1:c.1853T>A
(RAF1)
|
NP_001341618.1:p.Leu618His
|
|
|
NM_001354690.1:c.1793T>A
(RAF1)
|
NP_001341619.1:p.Leu598His
|
|
|
NM_001354691.1:c.1550T>A
(RAF1)
|
NP_001341620.1:p.Leu517His
|
|
|
NM_001354692.1:c.1550T>A
(RAF1)
|
NP_001341621.1:p.Leu517His
|
|
|
NM_001354693.1:c.1694T>A
(RAF1)
|
NP_001341622.1:p.Leu565His
|
|
|
NM_001354694.1:c.1610T>A
(RAF1)
|
NP_001341623.1:p.Leu537His
|
|
|
NM_001354695.1:c.1451T>A
(RAF1)
|
NP_001341624.1:p.Leu484His
|
|
|
NR_148940.1:n.2321T>A
(RAF1)
|
|
|
|
NR_148941.1:n.2267T>A
(RAF1)
|
|
|
|
NR_148942.1:n.2206T>A
(RAF1)
|
|
|
|
XM_011533974.3:c.1793T>A
(RAF1)
|
XP_011532276.1:p.Leu598His
|
|
|
XM_017006966.1:c.1694T>A
(RAF1)
|
XP_016862455.1:p.Leu565His
|
|
|
NM_001354689.3:c.1853T>A
(RAF1)
|
NP_001341618.1:p.Leu618His
|
|
|
NM_001354690.2:c.1793T>A
(RAF1)
|
NP_001341619.1:p.Leu598His
|
|
|
NM_001354691.2:c.1550T>A
(RAF1)
|
NP_001341620.1:p.Leu517His
|
|
|
NM_001354692.2:c.1550T>A
(RAF1)
|
NP_001341621.1:p.Leu517His
|
|
|
NM_001354693.2:c.1694T>A
(RAF1)
|
NP_001341622.1:p.Leu565His
|
|
|
NM_001354694.2:c.1610T>A
(RAF1)
|
NP_001341623.1:p.Leu537His
|
|
|
NM_001354695.2:c.1451T>A
(RAF1)
|
NP_001341624.1:p.Leu484His
|
|
|
NR_148940.2:n.2237T>A
(RAF1)
|
|
|
|
NR_148941.2:n.2183T>A
(RAF1)
|
|
|
|
NR_148942.2:n.2122T>A
(RAF1)
|
|
|
|
NM_001354690.3:c.1793T>A
(RAF1)
|
NP_001341619.1:p.Leu598His
|
|
|
NM_001354691.3:c.1550T>A
(RAF1)
|
NP_001341620.1:p.Leu517His
|
|
|
NM_001354692.3:c.1550T>A
(RAF1)
|
NP_001341621.1:p.Leu517His
|
|
|
NM_001354693.3:c.1694T>A
(RAF1)
|
NP_001341622.1:p.Leu565His
|
|
|
NM_001354694.3:c.1610T>A
(RAF1)
|
NP_001341623.1:p.Leu537His
|
|
|
NM_001354695.3:c.1451T>A
(RAF1)
|
NP_001341624.1:p.Leu484His
|
|
|
NM_002880.4:c.1793T>A
(RAF1)
MANE Select
|
NP_002871.1:p.Leu598His
|
|
|
NR_148940.3:n.2237T>A
(RAF1)
|
|
|
|
NR_148941.3:n.2183T>A
(RAF1)
|
|
|
|
NR_148942.3:n.2122T>A
(RAF1)
|
|
|
