|
ENST00000415788.3:c.983A>T
(SGCE)
|
ENSP00000405313.2:p.Glu328Val
|
|
|
ENST00000428696.7:c.854A>T
(SGCE)
|
ENSP00000397536.3:p.Glu285Val
|
|
|
ENST00000437425.7:c.752A>T
(SGCE)
|
ENSP00000394061.2:p.Glu251Val
|
|
|
ENST00000445866.7:c.875A>T
(SGCE)
|
ENSP00000398930.2:p.Glu292Val
|
|
|
ENST00000447873.6:c.875A>T
(SGCE)
|
ENSP00000388734.1:p.Glu292Val
|
|
|
ENST00000642169.1:c.*257A>T
(SGCE)
|
ENSP00000496346.1:n.*257A>T
|
|
|
ENST00000642291.1:c.736A>T
(SGCE)
|
|
|
|
ENST00000642353.1:n.846A>T
(SGCE)
|
|
|
|
ENST00000642394.1:c.752A>T
(SGCE)
|
ENSP00000493751.1:p.Glu251Val
|
|
|
ENST00000642441.1:c.956A>T
(SGCE)
|
ENSP00000495994.1:p.Glu319Val
|
|
|
ENST00000642497.1:n.1648A>T
(SGCE)
|
|
|
|
ENST00000642564.1:n.975A>T
(SGCE)
|
|
|
|
ENST00000642638.1:c.*913A>T
(SGCE)
|
ENSP00000495555.1:n.*913A>T
|
|
|
ENST00000642707.1:c.983A>T
(SGCE)
|
ENSP00000495270.1:p.Glu328Val
|
|
|
ENST00000642754.1:n.5747A>T
(SGCE)
|
|
|
|
ENST00000642759.1:n.964A>T
(SGCE)
|
|
|
|
ENST00000642802.1:n.697A>T
(SGCE)
|
|
|
|
ENST00000642904.1:n.963A>T
(SGCE)
|
|
|
|
ENST00000642933.1:c.875A>T
(SGCE)
|
ENSP00000496237.1:p.Glu292Val
|
|
|
ENST00000643020.1:c.801A>T
(SGCE)
|
|
|
|
ENST00000643041.1:c.875A>T
(SGCE)
|
ENSP00000495311.1:p.Glu292Val
|
|
|
ENST00000643128.1:c.875A>T
(SGCE)
|
ENSP00000496678.1:p.Glu292Val
|
|
|
ENST00000643160.1:c.106A>T
(SGCE)
|
|
|
|
ENST00000643193.1:c.875A>T
(SGCE)
|
ENSP00000496559.1:p.Glu292Val
|
|
|
ENST00000643206.1:c.*456A>T
(SGCE)
|
ENSP00000496172.1:n.*456A>T
|
|
|
ENST00000643272.1:c.983A>T
(SGCE)
|
ENSP00000494488.1:p.Glu328Val
|
|
|
ENST00000643324.1:n.1766A>T
(SGCE)
|
|
|
|
ENST00000643491.1:n.803A>T
(SGCE)
|
|
|
|
ENST00000643568.1:c.556A>T
(SGCE)
|
|
|
|
ENST00000643605.1:c.*862A>T
(SGCE)
|
ENSP00000496480.1:n.*862A>T
|
|
|
ENST00000643610.1:c.875A>T
(SGCE)
|
ENSP00000494350.1:p.Glu292Val
|
|
|
ENST00000643714.1:n.943A>T
(SGCE)
|
|
|
|
ENST00000643903.1:c.875A>T
(SGCE)
|
ENSP00000495165.1:p.Glu292Val
|
|
|
ENST00000643991.1:c.784A>T
(SGCE)
|
|
|
|
ENST00000644087.1:c.*952A>T
(SGCE)
|
ENSP00000495249.1:n.*952A>T
|
|
|
ENST00000644116.1:c.875A>T
(SGCE)
|
ENSP00000495276.1:p.Glu292Val
|
|
|
ENST00000644122.1:c.956A>T
(SGCE)
|
ENSP00000495236.1:p.Glu319Val
|
|
|
ENST00000644201.1:c.658A>T
(SGCE)
|
ENSP00000495044.1:n.658A>T
|
|
|
ENST00000644268.1:n.1495A>T
(SGCE)
|
|
|
|
ENST00000644373.1:n.1911A>T
(SGCE)
|
|
|
|
ENST00000644375.1:c.941A>T
(SGCE)
|
ENSP00000494315.1:p.Glu314Val
|
|
|
ENST00000644533.1:n.1630A>T
(SGCE)
|
|
|
|
ENST00000644551.1:c.956A>T
(SGCE)
|
ENSP00000493981.1:p.Glu319Val
|
|
|
ENST00000644609.1:c.875A>T
(SGCE)
|
ENSP00000496045.1:p.Glu292Val
|
|
|
ENST00000644639.1:c.*536A>T
(SGCE)
|
ENSP00000496391.1:n.*536A>T
|
|
|
ENST00000644658.1:c.390-1085A>T
(SGCE)
|
|
|
|
ENST00000644674.1:n.776A>T
(SGCE)
|
|
|
|
ENST00000644681.1:c.602A>T
(SGCE)
|
ENSP00000496455.1:p.Glu201Val
|
|
|
ENST00000644682.1:c.939A>T
(SGCE)
|
|
|
|
ENST00000644816.1:c.875A>T
(SGCE)
|
ENSP00000494898.1:p.Glu292Val
|
|
|
ENST00000644966.1:c.854A>T
(SGCE)
|
ENSP00000495105.1:n.854A>T
|
|
|
ENST00000645101.1:c.1064A>T
(SGCE)
|
ENSP00000494975.1:p.Glu355Val
|
|
|
ENST00000645109.1:c.983A>T
(SGCE)
|
ENSP00000495931.1:p.Glu328Val
|
|
|
ENST00000645262.1:c.752A>T
(SGCE)
|
ENSP00000494164.1:p.Glu251Val
|
|
|
ENST00000645445.1:c.849A>T
(SGCE)
|
|
|
|
ENST00000645535.1:c.602A>T
(SGCE)
|
ENSP00000493984.1:p.Glu201Val
|
|
|
ENST00000645579.1:n.1795A>T
(SGCE)
|
|
|
|
ENST00000645624.1:n.438A>T
(SGCE)
|
|
|
|
ENST00000645725.1:c.956A>T
(SGCE)
|
ENSP00000495480.1:p.Glu319Val
|
|
|
ENST00000646098.1:c.851A>T
(SGCE)
|
ENSP00000495591.1:p.Glu284Val
|
|
|
ENST00000646119.1:c.849A>T
(SGCE)
|
|
|
|
ENST00000646137.1:c.875A>T
(SGCE)
|
ENSP00000495199.1:p.Glu292Val
|
|
|
ENST00000646265.1:c.964A>T
(SGCE)
|
|
|
|
ENST00000646301.1:c.848A>T
(SGCE)
|
|
|
|
ENST00000646434.1:c.1124A>T
(SGCE)
|
|
|
|
ENST00000646466.1:c.*805A>T
(SGCE)
|
ENSP00000493511.1:n.*805A>T
|
|
|
ENST00000646489.1:c.983A>T
(SGCE)
|
ENSP00000496268.1:p.Glu328Val
|
|
|
ENST00000646559.1:c.*805A>T
(SGCE)
|
ENSP00000495838.1:n.*805A>T
|
|
|
ENST00000646600.1:c.*805A>T
(SGCE)
|
ENSP00000494041.1:n.*805A>T
|
|
|
ENST00000646682.1:c.*483A>T
(SGCE)
|
ENSP00000496461.1:n.*483A>T
|
|
|
ENST00000646879.1:c.875A>T
(SGCE)
|
ENSP00000495209.1:p.Glu292Val
|
|
|
ENST00000646910.1:n.908A>T
(SGCE)
|
|
|
|
ENST00000646943.1:c.875A>T
(SGCE)
|
ENSP00000494666.1:p.Glu292Val
|
|
|
ENST00000647018.1:c.983A>T
(SGCE)
|
ENSP00000493722.1:p.Glu328Val
|
|
|
ENST00000647031.1:n.3489A>T
(SGCE)
|
|
|
|
ENST00000647048.1:c.699A>T
(SGCE)
|
|
|
|
ENST00000647096.1:c.983A>T
(SGCE)
|
ENSP00000494192.1:p.Glu328Val
|
|
|
ENST00000647110.1:c.881A>T
(SGCE)
|
ENSP00000494738.1:p.Glu294Val
|
|
|
ENST00000647334.1:c.981A>T
(SGCE)
|
|
|
|
ENST00000647351.1:c.956A>T
(SGCE)
|
ENSP00000494556.1:p.Glu319Val
|
|
|
ENST00000647379.1:n.88A>T
(SGCE)
|
|
|
|
ENST00000647533.1:n.1574A>T
(SGCE)
|
|
|
|
ENST00000648936.2:c.875A>T
(SGCE)
MANE Select
|
ENSP00000497130.1:p.Glu292Val
|
|
|
ENST00000265735.11:c.875A>T
(SGCE)
|
ENSP00000265735.6:p.Glu292Val
|
|
|
ENST00000415788.2:c.983A>T
(SGCE)
|
ENSP00000405313.2:p.Glu328Val
|
|
|
ENST00000428696.6:c.875A>T
(SGCE)
|
ENSP00000397536.2:p.Glu292Val
|
|
|
ENST00000437425.6:c.752A>T
(SGCE)
|
ENSP00000394061.2:p.Glu251Val
|
|
|
ENST00000445866.6:c.875A>T
(SGCE)
|
ENSP00000398930.2:p.Glu292Val
|
|
|
ENST00000447873.5:c.875A>T
(SGCE)
|
ENSP00000388734.1:p.Glu292Val
|
|
|
ENST00000462731.1:n.168A>T
(SGCE)
|
|
|
|
NM_001099400.1:c.875A>T
(SGCE)
|
NP_001092870.1:p.Glu292Val
|
|
|
NM_001099401.1:c.875A>T
(SGCE)
|
NP_001092871.1:p.Glu292Val
|
|
|
NM_001301139.1:c.752A>T
(SGCE)
|
NP_001288068.1:p.Glu251Val
|
|
|
NM_003919.2:c.875A>T
(SGCE)
|
NP_003910.1:p.Glu292Val
|
|
|
XM_005250675.3:c.983A>T
(SGCE)
|
XP_005250732.1:p.Glu328Val
|
|
|
XM_005250677.3:c.983A>T
(SGCE)
|
XP_005250734.1:p.Glu328Val
|
|
|
XM_011516495.1:c.2128-30508T>A
(CASD1)
|
XP_011514797.1:n.2128-30508T>A
|
|
|
XM_011516663.1:c.983A>T
(SGCE)
|
XP_011514965.1:p.Glu328Val
|
|
|
XM_011516664.1:c.983A>T
(SGCE)
|
XP_011514966.1:p.Glu328Val
|
|
|
XM_011516665.1:c.875A>T
(SGCE)
|
XP_011514967.1:p.Glu292Val
|
|
|
XM_011516666.1:c.875A>T
(SGCE)
|
XP_011514968.1:p.Glu292Val
|
|
|
XM_011516667.1:c.788A>T
(SGCE)
|
XP_011514969.1:p.Glu263Val
|
|
|
XM_011516668.1:c.752A>T
(SGCE)
|
XP_011514970.1:p.Glu251Val
|
|
|
XM_011516669.1:c.602A>T
(SGCE)
|
XP_011514971.1:p.Glu201Val
|
|
|
NM_001346713.1:c.983A>T
(SGCE)
|
NP_001333642.1:p.Glu328Val
|
|
|
NM_001346715.1:c.983A>T
(SGCE)
|
NP_001333644.1:p.Glu328Val
|
|
|
NM_001346717.1:c.875A>T
(SGCE)
|
NP_001333646.1:p.Glu292Val
|
|
|
NM_001346719.1:c.788A>T
(SGCE)
|
NP_001333648.1:p.Glu263Val
|
|
|
NM_001346720.1:c.602A>T
(SGCE)
|
NP_001333649.1:p.Glu201Val
|
|
|
NM_001362807.1:c.788A>T
(SGCE)
|
NP_001349736.1:p.Glu263Val
|
|
|
NM_001362808.1:c.602A>T
(SGCE)
|
NP_001349737.1:p.Glu201Val
|
|
|
NM_001362809.1:c.752A>T
(SGCE)
|
NP_001349738.1:p.Glu251Val
|
|
|
XM_011516495.2:c.2128-30508T>A
(CASD1)
|
XP_011514797.1:n.2128-30508T>A
|
|
|
XM_011516663.2:c.983A>T
(SGCE)
|
XP_011514965.1:p.Glu328Val
|
|
|
XM_011516664.2:c.983A>T
(SGCE)
|
XP_011514966.1:p.Glu328Val
|
|
|
XM_011516665.3:c.875A>T
(SGCE)
|
XP_011514967.1:p.Glu292Val
|
|
|
XM_011516666.3:c.875A>T
(SGCE)
|
XP_011514968.1:p.Glu292Val
|
|
|
XM_011516667.2:c.788A>T
(SGCE)
|
XP_011514969.1:p.Glu263Val
|
|
|
XM_011516669.3:c.602A>T
(SGCE)
|
XP_011514971.1:p.Glu201Val
|
|
|
XM_017012763.1:c.788A>T
(SGCE)
|
XP_016868252.1:p.Glu263Val
|
|
|
XM_017012767.1:c.602A>T
(SGCE)
|
XP_016868256.1:p.Glu201Val
|
|
|
XM_024446985.1:c.752A>T
(SGCE)
|
XP_024302753.1:p.Glu251Val
|
|
|
XM_024446986.1:c.752A>T
(SGCE)
|
XP_024302754.1:p.Glu251Val
|
|
|
NM_001099400.2:c.875A>T
(SGCE)
|
NP_001092870.1:p.Glu292Val
|
|
|
NM_001099401.2:c.875A>T
(SGCE)
|
NP_001092871.1:p.Glu292Val
|
|
|
NM_001301139.2:c.752A>T
(SGCE)
|
NP_001288068.1:p.Glu251Val
|
|
|
NM_001346713.2:c.983A>T
(SGCE)
|
NP_001333642.1:p.Glu328Val
|
|
|
NM_001346715.2:c.983A>T
(SGCE)
|
NP_001333644.1:p.Glu328Val
|
|
|
NM_001346717.2:c.875A>T
(SGCE)
|
NP_001333646.1:p.Glu292Val
|
|
|
NM_001346719.2:c.788A>T
(SGCE)
|
NP_001333648.1:p.Glu263Val
|
|
|
NM_001346720.2:c.602A>T
(SGCE)
|
NP_001333649.1:p.Glu201Val
|
|
|
NM_001362807.2:c.788A>T
(SGCE)
|
NP_001349736.1:p.Glu263Val
|
|
|
NM_001362808.2:c.602A>T
(SGCE)
|
NP_001349737.1:p.Glu201Val
|
|
|
NM_001362809.2:c.752A>T
(SGCE)
|
NP_001349738.1:p.Glu251Val
|
|
|
NM_003919.3:c.875A>T
(SGCE)
MANE Select
|
NP_003910.1:p.Glu292Val
|
|
