|
ENST00000415788.3:c.1342C>T
(SGCE)
|
ENSP00000405313.2:p.Pro448Ser
|
|
|
ENST00000428696.7:c.1186C>T
(SGCE)
|
ENSP00000397536.3:p.Pro396Ser
|
|
|
ENST00000437425.7:c.1111C>T
(SGCE)
|
ENSP00000394061.2:p.Pro371Ser
|
|
|
ENST00000445866.7:c.1234C>T
(SGCE)
|
ENSP00000398930.2:p.Pro412Ser
|
|
|
ENST00000447873.6:c.1207C>T
(SGCE)
|
ENSP00000388734.1:p.Pro403Ser
|
|
|
ENST00000642291.1:c.1169C>T
(SGCE)
|
|
|
|
ENST00000642353.1:n.1205C>T
(SGCE)
|
|
|
|
ENST00000642394.1:c.1084C>T
(SGCE)
|
ENSP00000493751.1:p.Pro362Ser
|
|
|
ENST00000642441.1:c.1288C>T
(SGCE)
|
ENSP00000495994.1:p.Pro430Ser
|
|
|
ENST00000642497.1:n.1980C>T
(SGCE)
|
|
|
|
ENST00000642564.1:n.1334C>T
(SGCE)
|
|
|
|
ENST00000642638.1:c.*1272C>T
(SGCE)
|
ENSP00000495555.1:n.*1272C>T
|
|
|
ENST00000642707.1:c.1315C>T
(SGCE)
|
ENSP00000495270.1:p.Pro439Ser
|
|
|
ENST00000642754.1:n.6106C>T
(SGCE)
|
|
|
|
ENST00000642759.1:n.1296C>T
(SGCE)
|
|
|
|
ENST00000642802.1:n.1029C>T
(SGCE)
|
|
|
|
ENST00000642904.1:n.1295C>T
(SGCE)
|
|
|
|
ENST00000642933.1:c.1207C>T
(SGCE)
|
ENSP00000496237.1:p.Pro403Ser
|
|
|
ENST00000643020.1:c.1160C>T
(SGCE)
|
|
|
|
ENST00000643041.1:c.*195C>T
(SGCE)
|
ENSP00000495311.1:n.*195C>T
|
|
|
ENST00000643128.1:c.1234C>T
(SGCE)
|
ENSP00000496678.1:p.Pro412Ser
|
|
|
ENST00000643160.1:c.465C>T
(SGCE)
|
|
|
|
ENST00000643193.1:c.1207C>T
(SGCE)
|
ENSP00000496559.1:p.Pro403Ser
|
|
|
ENST00000643206.1:c.*815C>T
(SGCE)
|
ENSP00000496172.1:n.*815C>T
|
|
|
ENST00000643272.1:c.1315C>T
(SGCE)
|
ENSP00000494488.1:p.Pro439Ser
|
|
|
ENST00000643324.1:n.2125C>T
(SGCE)
|
|
|
|
ENST00000643491.1:n.1135C>T
(SGCE)
|
|
|
|
ENST00000643568.1:c.888C>T
(SGCE)
|
|
|
|
ENST00000643605.1:c.*1194C>T
(SGCE)
|
ENSP00000496480.1:n.*1194C>T
|
|
|
ENST00000643610.1:c.1234C>T
(SGCE)
|
ENSP00000494350.1:p.Pro412Ser
|
|
|
ENST00000643714.1:n.1275C>T
(SGCE)
|
|
|
|
ENST00000643903.1:c.1207C>T
(SGCE)
|
ENSP00000495165.1:p.Pro403Ser
|
|
|
ENST00000643991.1:c.1116C>T
(SGCE)
|
|
|
|
ENST00000644087.1:c.*1284C>T
(SGCE)
|
ENSP00000495249.1:n.*1284C>T
|
|
|
ENST00000644116.1:c.1207C>T
(SGCE)
|
ENSP00000495276.1:p.Pro403Ser
|
|
|
ENST00000644122.1:c.1315C>T
(SGCE)
|
ENSP00000495236.1:p.Pro439Ser
|
|
|
ENST00000644268.1:n.1827C>T
(SGCE)
|
|
|
|
ENST00000644373.1:n.2243C>T
(SGCE)
|
|
|
|
ENST00000644375.1:c.1273C>T
(SGCE)
|
ENSP00000494315.1:p.Pro425Ser
|
|
|
ENST00000644533.1:n.1989C>T
(SGCE)
|
|
|
|
ENST00000644551.1:c.1315C>T
(SGCE)
|
ENSP00000493981.1:p.Pro439Ser
|
|
|
ENST00000644609.1:c.1207C>T
(SGCE)
|
ENSP00000496045.1:p.Pro403Ser
|
|
|
ENST00000644639.1:c.*868C>T
(SGCE)
|
ENSP00000496391.1:n.*868C>T
|
|
|
ENST00000644658.1:c.586C>T
(SGCE)
|
|
|
|
ENST00000644674.1:n.1135C>T
(SGCE)
|
|
|
|
ENST00000644681.1:c.934C>T
(SGCE)
|
ENSP00000496455.1:p.Pro312Ser
|
|
|
ENST00000644682.1:c.1271C>T
(SGCE)
|
|
|
|
ENST00000644816.1:c.1234C>T
(SGCE)
|
ENSP00000494898.1:p.Pro412Ser
|
|
|
ENST00000645101.1:c.1396C>T
(SGCE)
|
ENSP00000494975.1:p.Pro466Ser
|
|
|
ENST00000645109.1:c.1342C>T
(SGCE)
|
ENSP00000495931.1:p.Pro448Ser
|
|
|
ENST00000645262.1:c.1084C>T
(SGCE)
|
ENSP00000494164.1:p.Pro362Ser
|
|
|
ENST00000645445.1:c.1181C>T
(SGCE)
|
|
|
|
ENST00000645535.1:c.934C>T
(SGCE)
|
ENSP00000493984.1:p.Pro312Ser
|
|
|
ENST00000645579.1:n.2127C>T
(SGCE)
|
|
|
|
ENST00000645624.1:n.770C>T
(SGCE)
|
|
|
|
ENST00000645665.1:n.453C>T
(SGCE)
|
|
|
|
ENST00000645725.1:c.1288C>T
(SGCE)
|
ENSP00000495480.1:p.Pro430Ser
|
|
|
ENST00000645804.1:c.56+903C>T
(SGCE)
|
ENSP00000494688.1:n.56+903C>T
|
|
|
ENST00000646098.1:c.1210C>T
(SGCE)
|
ENSP00000495591.1:p.Pro404Ser
|
|
|
ENST00000646119.1:c.1208C>T
(SGCE)
|
|
|
|
ENST00000646137.1:c.1207C>T
(SGCE)
|
ENSP00000495199.1:p.Pro403Ser
|
|
|
ENST00000646265.1:c.1296C>T
(SGCE)
|
|
|
|
ENST00000646301.1:c.1180C>T
(SGCE)
|
|
|
|
ENST00000646434.1:c.1456C>T
(SGCE)
|
|
|
|
ENST00000646466.1:c.*1137C>T
(SGCE)
|
ENSP00000493511.1:n.*1137C>T
|
|
|
ENST00000646489.1:c.1342C>T
(SGCE)
|
ENSP00000496268.1:p.Pro448Ser
|
|
|
ENST00000646559.1:c.*1164C>T
(SGCE)
|
ENSP00000495838.1:n.*1164C>T
|
|
|
ENST00000646600.1:c.*1137C>T
(SGCE)
|
ENSP00000494041.1:n.*1137C>T
|
|
|
ENST00000646879.1:c.1207C>T
(SGCE)
|
ENSP00000495209.1:p.Pro403Ser
|
|
|
ENST00000646910.1:n.1267C>T
(SGCE)
|
|
|
|
ENST00000646943.1:c.1234C>T
(SGCE)
|
ENSP00000494666.1:p.Pro412Ser
|
|
|
ENST00000647018.1:c.1342C>T
(SGCE)
|
ENSP00000493722.1:p.Pro448Ser
|
|
|
ENST00000647031.1:n.3821C>T
(SGCE)
|
|
|
|
ENST00000647048.1:c.1031C>T
(SGCE)
|
|
|
|
ENST00000647096.1:c.1342C>T
(SGCE)
|
ENSP00000494192.1:p.Pro448Ser
|
|
|
ENST00000647110.1:c.1213C>T
(SGCE)
|
ENSP00000494738.1:p.Pro405Ser
|
|
|
ENST00000647334.1:c.1313C>T
(SGCE)
|
|
|
|
ENST00000647351.1:c.1315C>T
(SGCE)
|
ENSP00000494556.1:p.Pro439Ser
|
|
|
ENST00000647379.1:n.447C>T
(SGCE)
|
|
|
|
ENST00000647533.1:n.2855C>T
(SGCE)
|
|
|
|
ENST00000648936.2:c.1234C>T
(SGCE)
MANE Select
|
ENSP00000497130.1:p.Pro412Ser
|
|
|
ENST00000265735.11:c.1234C>T
(SGCE)
|
ENSP00000265735.6:p.Pro412Ser
|
|
|
ENST00000415788.2:c.1342C>T
(SGCE)
|
ENSP00000405313.2:p.Pro448Ser
|
|
|
ENST00000428696.6:c.1207C>T
(SGCE)
|
ENSP00000397536.2:p.Pro403Ser
|
|
|
ENST00000437425.6:c.1111C>T
(SGCE)
|
ENSP00000394061.2:p.Pro371Ser
|
|
|
ENST00000445866.6:c.1234C>T
(SGCE)
|
ENSP00000398930.2:p.Pro412Ser
|
|
|
ENST00000447873.5:c.1207C>T
(SGCE)
|
ENSP00000388734.1:p.Pro403Ser
|
|
|
ENST00000472326.2:n.344C>T
(SGCE)
|
|
|
|
ENST00000522045.5:c.122+903C>T
(SGCE)
|
ENSP00000431080.1:n.122+903C>T
|
|
|
NM_001099400.1:c.1207C>T
(SGCE)
|
NP_001092870.1:p.Pro403Ser
|
|
|
NM_001099401.1:c.1234C>T
(SGCE)
|
NP_001092871.1:p.Pro412Ser
|
|
|
NM_001301139.1:c.1111C>T
(SGCE)
|
NP_001288068.1:p.Pro371Ser
|
|
|
NM_003919.2:c.1234C>T
(SGCE)
|
NP_003910.1:p.Pro412Ser
|
|
|
XM_005250675.3:c.1342C>T
(SGCE)
|
XP_005250732.1:p.Pro448Ser
|
|
|
XM_005250677.3:c.1315C>T
(SGCE)
|
XP_005250734.1:p.Pro439Ser
|
|
|
XM_011516495.1:c.2128-32522G>A
(CASD1)
|
XP_011514797.1:n.2128-32522G>A
|
|
|
XM_011516663.1:c.1342C>T
(SGCE)
|
XP_011514965.1:p.Pro448Ser
|
|
|
XM_011516664.1:c.1315C>T
(SGCE)
|
XP_011514966.1:p.Pro439Ser
|
|
|
XM_011516665.1:c.1234C>T
(SGCE)
|
XP_011514967.1:p.Pro412Ser
|
|
|
XM_011516666.1:c.1207C>T
(SGCE)
|
XP_011514968.1:p.Pro403Ser
|
|
|
XM_011516667.1:c.1147C>T
(SGCE)
|
XP_011514969.1:p.Pro383Ser
|
|
|
XM_011516668.1:c.1111C>T
(SGCE)
|
XP_011514970.1:p.Pro371Ser
|
|
|
XM_011516669.1:c.961C>T
(SGCE)
|
XP_011514971.1:p.Pro321Ser
|
|
|
NM_001346713.1:c.1342C>T
(SGCE)
|
NP_001333642.1:p.Pro448Ser
|
|
|
NM_001346715.1:c.1315C>T
(SGCE)
|
NP_001333644.1:p.Pro439Ser
|
|
|
NM_001346717.1:c.1207C>T
(SGCE)
|
NP_001333646.1:p.Pro403Ser
|
|
|
NM_001346719.1:c.1147C>T
(SGCE)
|
NP_001333648.1:p.Pro383Ser
|
|
|
NM_001346720.1:c.961C>T
(SGCE)
|
NP_001333649.1:p.Pro321Ser
|
|
|
NM_001362807.1:c.1120C>T
(SGCE)
|
NP_001349736.1:p.Pro374Ser
|
|
|
NM_001362808.1:c.934C>T
(SGCE)
|
NP_001349737.1:p.Pro312Ser
|
|
|
NM_001362809.1:c.1084C>T
(SGCE)
|
NP_001349738.1:p.Pro362Ser
|
|
|
XM_011516495.2:c.2128-32522G>A
(CASD1)
|
XP_011514797.1:n.2128-32522G>A
|
|
|
XM_011516663.2:c.1342C>T
(SGCE)
|
XP_011514965.1:p.Pro448Ser
|
|
|
XM_011516664.2:c.1315C>T
(SGCE)
|
XP_011514966.1:p.Pro439Ser
|
|
|
XM_011516665.3:c.1234C>T
(SGCE)
|
XP_011514967.1:p.Pro412Ser
|
|
|
XM_011516666.3:c.1207C>T
(SGCE)
|
XP_011514968.1:p.Pro403Ser
|
|
|
XM_011516667.2:c.1147C>T
(SGCE)
|
XP_011514969.1:p.Pro383Ser
|
|
|
XM_011516669.3:c.961C>T
(SGCE)
|
XP_011514971.1:p.Pro321Ser
|
|
|
XM_017012763.1:c.1147C>T
(SGCE)
|
XP_016868252.1:p.Pro383Ser
|
|
|
XM_017012767.1:c.934C>T
(SGCE)
|
XP_016868256.1:p.Pro312Ser
|
|
|
XM_024446985.1:c.1111C>T
(SGCE)
|
XP_024302753.1:p.Pro371Ser
|
|
|
XM_024446986.1:c.1084C>T
(SGCE)
|
XP_024302754.1:p.Pro362Ser
|
|
|
NM_001099400.2:c.1207C>T
(SGCE)
|
NP_001092870.1:p.Pro403Ser
|
|
|
NM_001099401.2:c.1234C>T
(SGCE)
|
NP_001092871.1:p.Pro412Ser
|
|
|
NM_001301139.2:c.1111C>T
(SGCE)
|
NP_001288068.1:p.Pro371Ser
|
|
|
NM_001346713.2:c.1342C>T
(SGCE)
|
NP_001333642.1:p.Pro448Ser
|
|
|
NM_001346715.2:c.1315C>T
(SGCE)
|
NP_001333644.1:p.Pro439Ser
|
|
|
NM_001346717.2:c.1207C>T
(SGCE)
|
NP_001333646.1:p.Pro403Ser
|
|
|
NM_001346719.2:c.1147C>T
(SGCE)
|
NP_001333648.1:p.Pro383Ser
|
|
|
NM_001346720.2:c.961C>T
(SGCE)
|
NP_001333649.1:p.Pro321Ser
|
|
|
NM_001362807.2:c.1120C>T
(SGCE)
|
NP_001349736.1:p.Pro374Ser
|
|
|
NM_001362808.2:c.934C>T
(SGCE)
|
NP_001349737.1:p.Pro312Ser
|
|
|
NM_001362809.2:c.1084C>T
(SGCE)
|
NP_001349738.1:p.Pro362Ser
|
|
|
NM_003919.3:c.1234C>T
(SGCE)
MANE Select
|
NP_003910.1:p.Pro412Ser
|
|
