|
ENST00000341012.13:c.1957C>G
|
ENSP00000343034.7:p.His653Asp
|
|
|
ENST00000404875.7:n.2659C>G
|
|
|
|
ENST00000423007.6:c.2176C>G
|
ENSP00000404119.2:p.His726Asp
|
|
|
ENST00000677295.2:c.*2463C>G
|
ENSP00000504346.2:n.*2463C>G
|
|
|
ENST00000678264.2:c.*2302C>G
|
ENSP00000503157.2:n.*2302C>G
|
|
|
ENST00000682070.1:n.2429C>G
|
|
|
|
ENST00000682639.1:c.116C>G
|
|
|
|
ENST00000682813.1:n.2516C>G
|
|
|
|
ENST00000683231.1:c.116C>G
|
|
|
|
ENST00000683392.1:n.4711C>G
|
|
|
|
ENST00000683712.1:n.2524C>G
|
|
|
|
ENST00000683900.1:n.4019C>G
|
|
|
|
ENST00000684062.1:n.2785C>G
|
|
|
|
ENST00000684399.1:c.116C>G
|
|
|
|
ENST00000684579.1:n.3965C>G
|
|
|
|
ENST00000341012.12:c.1957C>G
|
ENSP00000343034.7:p.His653Asp
|
|
|
ENST00000372220.5:c.988C>G
|
ENSP00000361294.5:p.His330Asp
|
|
|
ENST00000372228.9:c.2185C>G
|
ENSP00000361302.3:p.His729Asp
|
|
|
ENST00000402686.8:c.2119C>G
MANE Select
|
ENSP00000385797.4:p.His707Asp
|
|
|
ENST00000676640.1:c.2119C>G
|
ENSP00000503281.1:p.His707Asp
|
|
|
ENST00000676803.1:c.1180C>G
|
ENSP00000503093.1:p.His394Asp
|
|
|
ENST00000676835.1:c.*1334C>G
|
ENSP00000502911.1:n.*1334C>G
|
|
|
ENST00000677029.1:c.1663C>G
|
ENSP00000502936.1:p.His555Asp
|
|
|
ENST00000677099.1:c.*1829C>G
|
ENSP00000504553.1:n.*1829C>G
|
|
|
ENST00000677216.1:c.1768C>G
|
ENSP00000503772.1:p.His590Asp
|
|
|
ENST00000677295.1:c.*1341C>G
|
ENSP00000504346.1:n.*1341C>G
|
|
|
ENST00000677444.1:c.2064C>G
|
|
|
|
ENST00000677586.1:n.1486C>G
|
|
|
|
ENST00000677626.1:c.1768C>G
|
ENSP00000503552.1:p.His590Asp
|
|
|
ENST00000677853.1:c.*1127C>G
|
ENSP00000503488.1:n.*1127C>G
|
|
|
ENST00000678264.1:c.*1496C>G
|
ENSP00000503157.1:n.*1496C>G
|
|
|
ENST00000678303.1:c.2029C>G
|
ENSP00000503696.1:p.His677Asp
|
|
|
ENST00000678366.1:c.*2368C>G
|
ENSP00000504353.1:n.*2368C>G
|
|
|
ENST00000678546.1:c.*2064C>G
|
ENSP00000503062.1:n.*2064C>G
|
|
|
ENST00000678548.1:c.*2258C>G
|
ENSP00000503934.1:n.*2258C>G
|
|
|
ENST00000678626.1:n.1955C>G
|
|
|
|
ENST00000678739.1:c.*2285C>G
|
ENSP00000503806.1:n.*2285C>G
|
|
|
ENST00000678833.1:c.*1871C>G
|
ENSP00000503893.1:n.*1871C>G
|
|
|
ENST00000679023.1:c.1957C>G
|
ENSP00000503718.1:p.His653Asp
|
|
|
ENST00000679076.1:c.1738C>G
|
|
|
|
ENST00000679111.1:c.*875C>G
|
ENSP00000504257.1:n.*875C>G
|
|
|
ENST00000679189.1:c.1768C>G
|
ENSP00000503356.1:p.His590Asp
|
|
|
ENST00000341012.11:c.1957C>G
|
ENSP00000343034.7:p.His653Asp
|
|
|
ENST00000372220.4:c.982C>G
|
ENSP00000361294.4:p.His328Asp
|
|
|
ENST00000372228.7:c.2185C>G
|
ENSP00000361302.3:p.His729Asp
|
|
|
ENST00000402686.7:c.2119C>G
|
ENSP00000385797.3:p.His707Asp
|
|
|
ENST00000404875.6:c.1768C>G
|
ENSP00000384531.2:p.His590Asp
|
|
|
ENST00000423007.5:c.2119C>G
|
ENSP00000404119.1:p.His707Asp
|
|
|
ENST00000485278.5:n.2669C>G
|
|
|
|
NM_001077365.1:c.2119C>G
|
NP_001070833.1:p.His707Asp
|
|
|
NM_001077366.1:c.1957C>G
|
NP_001070834.1:p.His653Asp
|
|
|
NM_001136113.1:c.2119C>G
|
NP_001129585.1:p.His707Asp
|
|
|
NM_001136114.1:c.1768C>G
|
NP_001129586.1:p.His590Asp
|
|
|
NM_007171.3:c.2185C>G
|
NP_009102.3:p.His729Asp
|
|
|
XM_005272156.1:c.2185C>G
|
XP_005272213.1:p.His729Asp
|
|
|
XM_005272158.1:c.2023C>G
|
XP_005272215.1:p.His675Asp
|
|
|
XM_005272159.1:c.1834C>G
|
XP_005272216.1:p.His612Asp
|
|
|
XM_005272162.1:c.988C>G
|
XP_005272219.1:p.His330Asp
|
|
|
XM_006716932.1:c.1834C>G
|
XP_006716995.1:p.His612Asp
|
|
|
XM_011518140.1:c.2038C>G
|
XP_011516442.1:p.His680Asp
|
|
|
XM_011518141.1:c.1972C>G
|
XP_011516443.1:p.His658Asp
|
|
|
XM_011518142.1:c.1876C>G
|
XP_011516444.1:p.His626Asp
|
|
|
XM_011518143.1:c.1870C>G
|
XP_011516445.1:p.His624Asp
|
|
|
XM_011518145.1:c.1729C>G
|
XP_011516447.1:p.His577Asp
|
|
|
XM_011518147.1:c.1057C>G
|
XP_011516449.1:p.His353Asp
|
|
|
XR_929703.1:n.2361C>G
|
|
|
|
NM_001353193.1:c.2185C>G
|
NP_001340122.1:p.His729Asp
|
|
|
NM_001353194.1:c.1957C>G
|
NP_001340123.1:p.His653Asp
|
|
|
NM_001353195.1:c.1768C>G
|
NP_001340124.1:p.His590Asp
|
|
|
NM_001353196.1:c.2029C>G
|
NP_001340125.1:p.His677Asp
|
|
|
NM_001353197.1:c.2023C>G
|
NP_001340126.1:p.His675Asp
|
|
|
NM_001353198.1:c.2023C>G
|
NP_001340127.1:p.His675Asp
|
|
|
NM_001353199.1:c.1834C>G
|
NP_001340128.1:p.His612Asp
|
|
|
NM_001353200.1:c.1663C>G
|
NP_001340129.1:p.His555Asp
|
|
|
NR_148391.1:n.2169C>G
|
|
|
|
NR_148392.1:n.2387C>G
|
|
|
|
NR_148393.1:n.2308C>G
|
|
|
|
NR_148394.1:n.2062C>G
|
|
|
|
NR_148395.1:n.2460C>G
|
|
|
|
NR_148396.1:n.2094C>G
|
|
|
|
NR_148397.1:n.2219C>G
|
|
|
|
NR_148398.1:n.2174C>G
|
|
|
|
NR_148399.1:n.2700C>G
|
|
|
|
NR_148400.1:n.2299C>G
|
|
|
|
XM_005272162.3:c.988C>G
|
XP_005272219.1:p.His330Asp
|
|
|
XM_006716932.2:c.1834C>G
|
XP_006716995.1:p.His612Asp
|
|
|
XM_011518140.2:c.2038C>G
|
XP_011516442.1:p.His680Asp
|
|
|
XM_011518141.2:c.1972C>G
|
XP_011516443.1:p.His658Asp
|
|
|
XM_011518142.2:c.1876C>G
|
XP_011516444.1:p.His626Asp
|
|
|
XM_011518143.2:c.1870C>G
|
XP_011516445.1:p.His624Asp
|
|
|
XM_011518145.2:c.1729C>G
|
XP_011516447.1:p.His577Asp
|
|
|
XM_017014205.2:c.988C>G
|
XP_016869694.1:p.His330Asp
|
|
|
XM_024447380.1:c.988C>G
|
XP_024303148.1:p.His330Asp
|
|
|
XM_024447381.1:c.1294C>G
|
XP_024303149.1:p.His432Asp
|
|
|
XM_024447382.1:c.988C>G
|
XP_024303150.1:p.His330Asp
|
|
|
XR_001746160.2:n.2289C>G
|
|
|
|
XR_001746162.2:n.2494C>G
|
|
|
|
XR_001746164.1:n.2211C>G
|
|
|
|
XR_001746166.2:n.2506C>G
|
|
|
|
NM_001077365.2:c.2119C>G
MANE Select
|
NP_001070833.1:p.His707Asp
|
|
|
NM_001077366.2:c.1957C>G
|
NP_001070834.1:p.His653Asp
|
|
|
NM_001136113.2:c.2119C>G
|
NP_001129585.1:p.His707Asp
|
|
|
NM_001136114.2:c.1768C>G
|
NP_001129586.1:p.His590Asp
|
|
|
NM_001353193.2:c.2185C>G
|
NP_001340122.2:p.His729Asp
|
|
|
NM_001353194.2:c.1957C>G
|
NP_001340123.1:p.His653Asp
|
|
|
NM_001353195.2:c.1768C>G
|
NP_001340124.1:p.His590Asp
|
|
|
NM_001353196.2:c.2029C>G
|
NP_001340125.1:p.His677Asp
|
|
|
NM_001353197.2:c.2023C>G
|
NP_001340126.2:p.His675Asp
|
|
|
NM_001353198.2:c.2023C>G
|
NP_001340127.2:p.His675Asp
|
|
|
NM_001353199.2:c.1834C>G
|
NP_001340128.2:p.His612Asp
|
|
|
NM_001353200.2:c.1663C>G
|
NP_001340129.1:p.His555Asp
|
|
|
NM_001374689.1:c.2107C>G
|
NP_001361618.1:p.His703Asp
|
|
|
NM_001374690.1:c.1900C>G
|
NP_001361619.1:p.His634Asp
|
|
|
NM_001374691.1:c.1768C>G
|
NP_001361620.1:p.His590Asp
|
|
|
NM_001374692.1:c.1768C>G
|
NP_001361621.1:p.His590Asp
|
|
|
NM_001374693.1:c.1768C>G
|
NP_001361622.1:p.His590Asp
|
|
|
NM_001374695.1:c.1729C>G
|
NP_001361624.1:p.His577Asp
|
|
|
NM_007171.4:c.2185C>G
|
NP_009102.4:p.His729Asp
|
|
|
NR_148391.2:n.2153C>G
|
|
|
|
NR_148392.2:n.2371C>G
|
|
|
|
NR_148393.2:n.2292C>G
|
|
|
|
NR_148394.2:n.2046C>G
|
|
|
|
NR_148395.2:n.2444C>G
|
|
|
|
NR_148396.2:n.2078C>G
|
|
|
|
NR_148397.2:n.2203C>G
|
|
|
|
NR_148398.2:n.2158C>G
|
|
|
|
NR_148399.2:n.2684C>G
|
|
|
|
NR_148400.2:n.2283C>G
|
|
|
