|
ENST00000415788.3:c.1097T>C
(SGCE)
|
ENSP00000405313.2:p.Val366Ala
|
|
|
ENST00000428696.7:c.968T>C
(SGCE)
|
ENSP00000397536.3:p.Val323Ala
|
|
|
ENST00000437425.7:c.866T>C
(SGCE)
|
ENSP00000394061.2:p.Val289Ala
|
|
|
ENST00000445866.7:c.989T>C
(SGCE)
|
ENSP00000398930.2:p.Val330Ala
|
|
|
ENST00000447873.6:c.989T>C
(SGCE)
|
ENSP00000388734.1:p.Val330Ala
|
|
|
ENST00000642169.1:c.*371T>C
(SGCE)
|
ENSP00000496346.1:n.*371T>C
|
|
|
ENST00000642291.1:c.850T>C
(SGCE)
|
|
|
|
ENST00000642353.1:n.960T>C
(SGCE)
|
|
|
|
ENST00000642394.1:c.866T>C
(SGCE)
|
ENSP00000493751.1:p.Val289Ala
|
|
|
ENST00000642441.1:c.1070T>C
(SGCE)
|
ENSP00000495994.1:p.Val357Ala
|
|
|
ENST00000642497.1:n.1762T>C
(SGCE)
|
|
|
|
ENST00000642564.1:n.1089T>C
(SGCE)
|
|
|
|
ENST00000642638.1:c.*1027T>C
(SGCE)
|
ENSP00000495555.1:n.*1027T>C
|
|
|
ENST00000642707.1:c.1097T>C
(SGCE)
|
ENSP00000495270.1:p.Val366Ala
|
|
|
ENST00000642754.1:n.5861T>C
(SGCE)
|
|
|
|
ENST00000642759.1:n.1078T>C
(SGCE)
|
|
|
|
ENST00000642802.1:n.811T>C
(SGCE)
|
|
|
|
ENST00000642904.1:n.1077T>C
(SGCE)
|
|
|
|
ENST00000642933.1:c.989T>C
(SGCE)
|
ENSP00000496237.1:p.Val330Ala
|
|
|
ENST00000643020.1:c.915T>C
(SGCE)
|
|
|
|
ENST00000643041.1:c.989T>C
(SGCE)
|
ENSP00000495311.1:p.Val330Ala
|
|
|
ENST00000643128.1:c.989T>C
(SGCE)
|
ENSP00000496678.1:p.Val330Ala
|
|
|
ENST00000643160.1:c.220T>C
(SGCE)
|
|
|
|
ENST00000643193.1:c.989T>C
(SGCE)
|
ENSP00000496559.1:p.Val330Ala
|
|
|
ENST00000643206.1:c.*570T>C
(SGCE)
|
ENSP00000496172.1:n.*570T>C
|
|
|
ENST00000643272.1:c.1097T>C
(SGCE)
|
ENSP00000494488.1:p.Val366Ala
|
|
|
ENST00000643324.1:n.1880T>C
(SGCE)
|
|
|
|
ENST00000643491.1:n.917T>C
(SGCE)
|
|
|
|
ENST00000643568.1:c.670T>C
(SGCE)
|
|
|
|
ENST00000643605.1:c.*976T>C
(SGCE)
|
ENSP00000496480.1:n.*976T>C
|
|
|
ENST00000643610.1:c.989T>C
(SGCE)
|
ENSP00000494350.1:p.Val330Ala
|
|
|
ENST00000643714.1:n.1057T>C
(SGCE)
|
|
|
|
ENST00000643903.1:c.989T>C
(SGCE)
|
ENSP00000495165.1:p.Val330Ala
|
|
|
ENST00000643991.1:c.898T>C
(SGCE)
|
|
|
|
ENST00000644087.1:c.*1066T>C
(SGCE)
|
ENSP00000495249.1:n.*1066T>C
|
|
|
ENST00000644116.1:c.989T>C
(SGCE)
|
ENSP00000495276.1:p.Val330Ala
|
|
|
ENST00000644122.1:c.1070T>C
(SGCE)
|
ENSP00000495236.1:p.Val357Ala
|
|
|
ENST00000644201.1:c.772T>C
(SGCE)
|
ENSP00000495044.1:n.772T>C
|
|
|
ENST00000644268.1:n.1609T>C
(SGCE)
|
|
|
|
ENST00000644373.1:n.2025T>C
(SGCE)
|
|
|
|
ENST00000644375.1:c.1055T>C
(SGCE)
|
ENSP00000494315.1:p.Val352Ala
|
|
|
ENST00000644533.1:n.1744T>C
(SGCE)
|
|
|
|
ENST00000644551.1:c.1070T>C
(SGCE)
|
ENSP00000493981.1:p.Val357Ala
|
|
|
ENST00000644609.1:c.989T>C
(SGCE)
|
ENSP00000496045.1:p.Val330Ala
|
|
|
ENST00000644639.1:c.*650T>C
(SGCE)
|
ENSP00000496391.1:n.*650T>C
|
|
|
ENST00000644658.1:c.390-971T>C
(SGCE)
|
|
|
|
ENST00000644674.1:n.890T>C
(SGCE)
|
|
|
|
ENST00000644681.1:c.716T>C
(SGCE)
|
ENSP00000496455.1:p.Val239Ala
|
|
|
ENST00000644682.1:c.1053T>C
(SGCE)
|
|
|
|
ENST00000644816.1:c.989T>C
(SGCE)
|
ENSP00000494898.1:p.Val330Ala
|
|
|
ENST00000645101.1:c.1178T>C
(SGCE)
|
ENSP00000494975.1:p.Val393Ala
|
|
|
ENST00000645109.1:c.1097T>C
(SGCE)
|
ENSP00000495931.1:p.Val366Ala
|
|
|
ENST00000645262.1:c.866T>C
(SGCE)
|
ENSP00000494164.1:p.Val289Ala
|
|
|
ENST00000645445.1:c.963T>C
(SGCE)
|
|
|
|
ENST00000645535.1:c.716T>C
(SGCE)
|
ENSP00000493984.1:p.Val239Ala
|
|
|
ENST00000645579.1:n.1909T>C
(SGCE)
|
|
|
|
ENST00000645624.1:n.552T>C
(SGCE)
|
|
|
|
ENST00000645725.1:c.1070T>C
(SGCE)
|
ENSP00000495480.1:p.Val357Ala
|
|
|
ENST00000646098.1:c.965T>C
(SGCE)
|
ENSP00000495591.1:p.Val322Ala
|
|
|
ENST00000646119.1:c.963T>C
(SGCE)
|
|
|
|
ENST00000646137.1:c.989T>C
(SGCE)
|
ENSP00000495199.1:p.Val330Ala
|
|
|
ENST00000646265.1:c.1078T>C
(SGCE)
|
|
|
|
ENST00000646301.1:c.962T>C
(SGCE)
|
|
|
|
ENST00000646434.1:c.1238T>C
(SGCE)
|
|
|
|
ENST00000646466.1:c.*919T>C
(SGCE)
|
ENSP00000493511.1:n.*919T>C
|
|
|
ENST00000646489.1:c.1097T>C
(SGCE)
|
ENSP00000496268.1:p.Val366Ala
|
|
|
ENST00000646559.1:c.*919T>C
(SGCE)
|
ENSP00000495838.1:n.*919T>C
|
|
|
ENST00000646600.1:c.*919T>C
(SGCE)
|
ENSP00000494041.1:n.*919T>C
|
|
|
ENST00000646682.1:c.*597T>C
(SGCE)
|
ENSP00000496461.1:n.*597T>C
|
|
|
ENST00000646879.1:c.989T>C
(SGCE)
|
ENSP00000495209.1:p.Val330Ala
|
|
|
ENST00000646910.1:n.1022T>C
(SGCE)
|
|
|
|
ENST00000646943.1:c.989T>C
(SGCE)
|
ENSP00000494666.1:p.Val330Ala
|
|
|
ENST00000647018.1:c.1097T>C
(SGCE)
|
ENSP00000493722.1:p.Val366Ala
|
|
|
ENST00000647031.1:n.3603T>C
(SGCE)
|
|
|
|
ENST00000647048.1:c.813T>C
(SGCE)
|
|
|
|
ENST00000647096.1:c.1097T>C
(SGCE)
|
ENSP00000494192.1:p.Val366Ala
|
|
|
ENST00000647110.1:c.995T>C
(SGCE)
|
ENSP00000494738.1:p.Val332Ala
|
|
|
ENST00000647334.1:c.1095T>C
(SGCE)
|
|
|
|
ENST00000647351.1:c.1070T>C
(SGCE)
|
ENSP00000494556.1:p.Val357Ala
|
|
|
ENST00000647379.1:n.202T>C
(SGCE)
|
|
|
|
ENST00000647533.1:n.1688T>C
(SGCE)
|
|
|
|
ENST00000648936.2:c.989T>C
(SGCE)
MANE Select
|
ENSP00000497130.1:p.Val330Ala
|
|
|
ENST00000265735.11:c.989T>C
(SGCE)
|
ENSP00000265735.6:p.Val330Ala
|
|
|
ENST00000415788.2:c.1097T>C
(SGCE)
|
ENSP00000405313.2:p.Val366Ala
|
|
|
ENST00000428696.6:c.989T>C
(SGCE)
|
ENSP00000397536.2:p.Val330Ala
|
|
|
ENST00000437425.6:c.866T>C
(SGCE)
|
ENSP00000394061.2:p.Val289Ala
|
|
|
ENST00000445866.6:c.989T>C
(SGCE)
|
ENSP00000398930.2:p.Val330Ala
|
|
|
ENST00000447873.5:c.989T>C
(SGCE)
|
ENSP00000388734.1:p.Val330Ala
|
|
|
ENST00000462731.1:n.282T>C
(SGCE)
|
|
|
|
ENST00000522045.5:c.47T>C
(SGCE)
|
ENSP00000431080.1:p.Val16Ala
|
|
|
NM_001099400.1:c.989T>C
(SGCE)
|
NP_001092870.1:p.Val330Ala
|
|
|
NM_001099401.1:c.989T>C
(SGCE)
|
NP_001092871.1:p.Val330Ala
|
|
|
NM_001301139.1:c.866T>C
(SGCE)
|
NP_001288068.1:p.Val289Ala
|
|
|
NM_003919.2:c.989T>C
(SGCE)
|
NP_003910.1:p.Val330Ala
|
|
|
XM_005250675.3:c.1097T>C
(SGCE)
|
XP_005250732.1:p.Val366Ala
|
|
|
XM_005250677.3:c.1097T>C
(SGCE)
|
XP_005250734.1:p.Val366Ala
|
|
|
XM_011516495.1:c.2128-30622A>G
(CASD1)
|
XP_011514797.1:n.2128-30622A>G
|
|
|
XM_011516663.1:c.1097T>C
(SGCE)
|
XP_011514965.1:p.Val366Ala
|
|
|
XM_011516664.1:c.1097T>C
(SGCE)
|
XP_011514966.1:p.Val366Ala
|
|
|
XM_011516665.1:c.989T>C
(SGCE)
|
XP_011514967.1:p.Val330Ala
|
|
|
XM_011516666.1:c.989T>C
(SGCE)
|
XP_011514968.1:p.Val330Ala
|
|
|
XM_011516667.1:c.902T>C
(SGCE)
|
XP_011514969.1:p.Val301Ala
|
|
|
XM_011516668.1:c.866T>C
(SGCE)
|
XP_011514970.1:p.Val289Ala
|
|
|
XM_011516669.1:c.716T>C
(SGCE)
|
XP_011514971.1:p.Val239Ala
|
|
|
NM_001346713.1:c.1097T>C
(SGCE)
|
NP_001333642.1:p.Val366Ala
|
|
|
NM_001346715.1:c.1097T>C
(SGCE)
|
NP_001333644.1:p.Val366Ala
|
|
|
NM_001346717.1:c.989T>C
(SGCE)
|
NP_001333646.1:p.Val330Ala
|
|
|
NM_001346719.1:c.902T>C
(SGCE)
|
NP_001333648.1:p.Val301Ala
|
|
|
NM_001346720.1:c.716T>C
(SGCE)
|
NP_001333649.1:p.Val239Ala
|
|
|
NM_001362807.1:c.902T>C
(SGCE)
|
NP_001349736.1:p.Val301Ala
|
|
|
NM_001362808.1:c.716T>C
(SGCE)
|
NP_001349737.1:p.Val239Ala
|
|
|
NM_001362809.1:c.866T>C
(SGCE)
|
NP_001349738.1:p.Val289Ala
|
|
|
XM_011516495.2:c.2128-30622A>G
(CASD1)
|
XP_011514797.1:n.2128-30622A>G
|
|
|
XM_011516663.2:c.1097T>C
(SGCE)
|
XP_011514965.1:p.Val366Ala
|
|
|
XM_011516664.2:c.1097T>C
(SGCE)
|
XP_011514966.1:p.Val366Ala
|
|
|
XM_011516665.3:c.989T>C
(SGCE)
|
XP_011514967.1:p.Val330Ala
|
|
|
XM_011516666.3:c.989T>C
(SGCE)
|
XP_011514968.1:p.Val330Ala
|
|
|
XM_011516667.2:c.902T>C
(SGCE)
|
XP_011514969.1:p.Val301Ala
|
|
|
XM_011516669.3:c.716T>C
(SGCE)
|
XP_011514971.1:p.Val239Ala
|
|
|
XM_017012763.1:c.902T>C
(SGCE)
|
XP_016868252.1:p.Val301Ala
|
|
|
XM_017012767.1:c.716T>C
(SGCE)
|
XP_016868256.1:p.Val239Ala
|
|
|
XM_024446985.1:c.866T>C
(SGCE)
|
XP_024302753.1:p.Val289Ala
|
|
|
XM_024446986.1:c.866T>C
(SGCE)
|
XP_024302754.1:p.Val289Ala
|
|
|
NM_001099400.2:c.989T>C
(SGCE)
|
NP_001092870.1:p.Val330Ala
|
|
|
NM_001099401.2:c.989T>C
(SGCE)
|
NP_001092871.1:p.Val330Ala
|
|
|
NM_001301139.2:c.866T>C
(SGCE)
|
NP_001288068.1:p.Val289Ala
|
|
|
NM_001346713.2:c.1097T>C
(SGCE)
|
NP_001333642.1:p.Val366Ala
|
|
|
NM_001346715.2:c.1097T>C
(SGCE)
|
NP_001333644.1:p.Val366Ala
|
|
|
NM_001346717.2:c.989T>C
(SGCE)
|
NP_001333646.1:p.Val330Ala
|
|
|
NM_001346719.2:c.902T>C
(SGCE)
|
NP_001333648.1:p.Val301Ala
|
|
|
NM_001346720.2:c.716T>C
(SGCE)
|
NP_001333649.1:p.Val239Ala
|
|
|
NM_001362807.2:c.902T>C
(SGCE)
|
NP_001349736.1:p.Val301Ala
|
|
|
NM_001362808.2:c.716T>C
(SGCE)
|
NP_001349737.1:p.Val239Ala
|
|
|
NM_001362809.2:c.866T>C
(SGCE)
|
NP_001349738.1:p.Val289Ala
|
|
|
NM_003919.3:c.989T>C
(SGCE)
MANE Select
|
NP_003910.1:p.Val330Ala
|
|
