|
ENST00000574886.2:n.1500T>G
|
|
|
|
ENST00000576677.6:n.1421T>G
|
|
|
|
ENST00000681983.1:n.2428T>G
|
|
|
|
ENST00000682099.1:n.1189T>G
|
|
|
|
ENST00000682213.1:c.*263T>G
|
ENSP00000508166.1:n.*263T>G
|
|
|
ENST00000682315.1:c.606T>G
|
ENSP00000507232.1:p.Leu202=
|
|
|
ENST00000682479.1:c.2382T>G
|
ENSP00000508214.1:p.Leu794=
|
|
|
ENST00000682610.1:n.1532T>G
|
|
|
|
ENST00000682654.1:c.*263T>G
|
ENSP00000507412.1:n.*263T>G
|
|
|
ENST00000682722.1:c.2241T>G
|
ENSP00000508364.1:p.Leu747=
|
|
|
ENST00000683041.1:c.*263T>G
|
ENSP00000506994.1:n.*263T>G
|
|
|
ENST00000683184.1:c.*1945T>G
|
ENSP00000507757.1:n.*1945T>G
|
|
|
ENST00000683282.1:c.2208T>G
|
ENSP00000506913.1:p.Leu736=
|
|
|
ENST00000683444.1:c.*1869T>G
|
ENSP00000507553.1:n.*1869T>G
|
|
|
ENST00000683584.1:n.1115T>G
|
|
|
|
ENST00000683821.1:c.606T>G
|
ENSP00000507651.1:p.Leu202=
|
|
|
ENST00000683839.1:n.1746T>G
|
|
|
|
ENST00000684000.1:c.2376T>G
|
ENSP00000506795.1:p.Leu792=
|
|
|
ENST00000684188.1:c.2103T>G
|
ENSP00000507153.1:p.Leu701=
|
|
|
ENST00000684349.1:c.2478T>G
|
ENSP00000508067.1:p.Leu826=
|
|
|
ENST00000684361.1:c.2292T>G
|
ENSP00000507364.1:p.Leu764=
|
|
|
ENST00000684408.1:c.1935T>G
|
ENSP00000506837.1:p.Leu645=
|
|
|
ENST00000684429.1:c.2220T>G
|
ENSP00000507224.1:p.Leu740=
|
|
|
ENST00000684464.1:c.2385T>G
|
ENSP00000508333.1:p.Leu795=
|
|
|
ENST00000684544.1:c.2211T>G
|
ENSP00000507337.1:p.Leu737=
|
|
|
ENST00000684559.1:n.1047T>G
|
|
|
|
ENST00000684760.1:c.2559T>G
|
ENSP00000507696.1:p.Leu853=
|
|
|
ENST00000684776.1:c.*775T>G
|
ENSP00000507861.1:n.*775T>G
|
|
|
ENST00000355528.9:c.2292T>G
MANE Select
|
ENSP00000347719.4:p.Leu764=
|
|
|
ENST00000355528.8:c.2292T>G
|
ENSP00000347719.4:p.Leu764=
|
|
|
ENST00000539345.6:c.2292T>G
|
ENSP00000440671.2:p.Leu764=
|
|
|
ENST00000571618.5:n.470T>G
|
|
|
|
ENST00000571796.5:n.950T>G
|
|
|
|
ENST00000574422.1:c.606T>G
|
ENSP00000458599.1:p.Leu202=
|
|
|
ENST00000574818.5:n.350T>G
|
|
|
|
ENST00000574886.1:n.676T>G
|
|
|
|
ENST00000574975.5:c.669T>G
|
ENSP00000461680.1:p.Leu223=
|
|
|
ENST00000576760.5:c.606T>G
|
ENSP00000460949.1:p.Leu202=
|
|
|
NM_005993.4:c.2292T>G
|
NP_005984.3:p.Leu764=
|
|
|
XM_005256396.3:c.2241T>G
|
XP_005256453.1:p.Leu747=
|
|
|
XM_005256399.3:c.1008T>G
|
XP_005256456.1:p.Leu336=
|
|
|
XM_005256400.3:c.606T>G
|
XP_005256457.1:p.Leu202=
|
|
|
XM_005256401.3:c.606T>G
|
XP_005256458.1:p.Leu202=
|
|
|
XM_005256402.3:c.606T>G
|
XP_005256459.1:p.Leu202=
|
|
|
XM_005256403.3:c.606T>G
|
XP_005256460.1:p.Leu202=
|
|
|
XM_005256404.3:c.606T>G
|
XP_005256461.1:p.Leu202=
|
|
|
XM_006722290.2:c.2211T>G
|
XP_006722353.1:p.Leu737=
|
|
|
XM_006722291.2:c.996T>G
|
XP_006722354.1:p.Leu332=
|
|
|
XM_006722292.2:c.606T>G
|
XP_006722355.1:p.Leu202=
|
|
|
XM_011523589.1:c.1947T>G
|
XP_011521891.1:p.Leu649=
|
|
|
XM_011523590.1:c.1935T>G
|
XP_011521892.1:p.Leu645=
|
|
|
XM_011523591.1:c.1932T>G
|
XP_011521893.1:p.Leu644=
|
|
|
XM_011523592.1:c.1845T>G
|
XP_011521894.1:p.Leu615=
|
|
|
XM_011523593.1:c.1539T>G
|
XP_011521895.1:p.Leu513=
|
|
|
XM_011523594.1:c.1020T>G
|
XP_011521896.1:p.Leu340=
|
|
|
XM_011523595.1:c.987T>G
|
XP_011521897.1:p.Leu329=
|
|
|
XM_011523596.1:c.*23T>G
|
XP_011521898.1:n.*23T>G
|
|
|
XM_011523597.1:c.753T>G
|
XP_011521899.1:p.Leu251=
|
|
|
XM_011523598.1:c.750T>G
|
XP_011521900.1:p.Leu250=
|
|
|
XM_011523599.1:c.744T>G
|
XP_011521901.1:p.Leu248=
|
|
|
XM_011523600.1:c.606T>G
|
XP_011521902.1:p.Leu202=
|
|
|
XR_430033.2:n.2400T>G
|
|
|
|
XM_005256396.4:c.2241T>G
|
XP_005256453.1:p.Leu747=
|
|
|
XM_005256399.5:c.1008T>G
|
XP_005256456.1:p.Leu336=
|
|
|
XM_005256404.4:c.606T>G
|
XP_005256461.1:p.Leu202=
|
|
|
XM_006722291.4:c.996T>G
|
XP_006722354.1:p.Leu332=
|
|
|
XM_006722292.3:c.606T>G
|
XP_006722355.1:p.Leu202=
|
|
|
XM_011523589.2:c.1947T>G
|
XP_011521891.1:p.Leu649=
|
|
|
XM_011523591.2:c.1932T>G
|
XP_011521893.1:p.Leu644=
|
|
|
XM_011523593.2:c.1539T>G
|
XP_011521895.1:p.Leu513=
|
|
|
XM_011523594.2:c.1020T>G
|
XP_011521896.1:p.Leu340=
|
|
|
XM_011523595.3:c.987T>G
|
XP_011521897.1:p.Leu329=
|
|
|
XM_011523597.2:c.753T>G
|
XP_011521899.1:p.Leu251=
|
|
|
XM_011523599.2:c.744T>G
|
XP_011521901.1:p.Leu248=
|
|
|
XM_011523600.3:c.606T>G
|
XP_011521902.1:p.Leu202=
|
|
|
XM_017024987.1:c.2103T>G
|
XP_016880476.1:p.Leu701=
|
|
|
XM_017024989.1:c.654T>G
|
XP_016880478.1:p.Leu218=
|
|
|
XM_017024990.2:c.606T>G
|
XP_016880479.1:p.Leu202=
|
|
|
XM_024450899.1:c.606T>G
|
XP_024306667.1:p.Leu202=
|
|
|
XM_024450900.1:c.606T>G
|
XP_024306668.1:p.Leu202=
|
|
|
XM_024450901.1:c.606T>G
|
XP_024306669.1:p.Leu202=
|
|
|
XM_024450902.1:c.606T>G
|
XP_024306670.1:p.Leu202=
|
|
|
XR_001752597.1:n.2400T>G
|
|
|
|
XR_001752598.1:n.2400T>G
|
|
|
|
XR_001752599.1:n.2400T>G
|
|
|
|
XR_001752600.1:n.2318T>G
|
|
|
|
NM_005993.5:c.2292T>G
MANE Select
|
NP_005984.3:p.Leu764=
|
|
