|
ENST00000484552.6:c.819G>T
(CAST)
|
ENSP00000432878.2:p.Thr273=
|
|
|
ENST00000508608.6:c.1749G>T
(CAST)
|
ENSP00000422677.2:p.Thr583=
|
|
|
ENST00000510756.6:c.1527G>T
(CAST)
|
ENSP00000422176.2:p.Thr509=
|
|
|
ENST00000674587.1:c.1356G>T
(CAST)
|
ENSP00000501797.1:p.Thr452=
|
|
|
ENST00000674702.1:c.1641G>T
(CAST)
|
ENSP00000502345.1:p.Thr547=
|
|
|
ENST00000674984.1:c.1833G>T
(CAST)
|
ENSP00000501713.1:p.Thr611=
|
|
|
ENST00000675033.1:c.1527G>T
(CAST)
|
ENSP00000501659.1:p.Thr509=
|
|
|
ENST00000675179.1:c.1899G>T
(CAST)
MANE Select
|
ENSP00000501872.1:p.Thr633=
|
|
|
ENST00000675185.1:c.280G>T
(CAST)
|
|
|
|
ENST00000675266.1:c.1801G>T
(CAST)
|
|
|
|
ENST00000675267.1:c.*1523G>T
(CAST)
|
ENSP00000502095.1:n.*1523G>T
|
|
|
ENST00000675275.1:c.616G>T
(CAST)
|
|
|
|
ENST00000675479.1:c.1512G>T
(CAST)
|
ENSP00000502244.1:p.Thr504=
|
|
|
ENST00000675614.1:c.1569G>T
(CAST)
|
ENSP00000502136.1:p.Thr523=
|
|
|
ENST00000675663.1:c.1788G>T
(CAST)
|
ENSP00000502449.1:p.Thr596=
|
|
|
ENST00000675734.1:n.443G>T
(CAST)
|
|
|
|
ENST00000675858.1:c.1443G>T
(CAST)
|
ENSP00000501780.1:p.Thr481=
|
|
|
ENST00000296754.7:c.*861C>A
(ERAP1)
|
ENSP00000296754.3:n.*861C>A
|
|
|
ENST00000309190.9:c.1584G>T
(CAST)
|
ENSP00000312523.5:p.Thr528=
|
|
|
ENST00000325674.11:c.819G>T
(CAST)
|
ENSP00000320319.8:p.Thr273=
|
|
|
ENST00000338252.7:c.1611G>T
(CAST)
|
ENSP00000343421.3:p.Thr537=
|
|
|
ENST00000341926.7:c.1650G>T
(CAST)
|
ENSP00000339914.3:p.Thr550=
|
|
|
ENST00000348386.7:n.1592G>T
(CAST)
|
|
|
|
ENST00000395812.6:c.1776G>T
(CAST)
|
ENSP00000379157.2:p.Thr592=
|
|
|
ENST00000395813.5:c.1650G>T
(CAST)
|
ENSP00000379158.2:p.Thr550=
|
|
|
ENST00000437034.6:c.905G>T
(CAST)
|
|
|
|
ENST00000484552.5:c.877G>T
(CAST)
|
|
|
|
ENST00000504465.5:c.1434G>T
(CAST)
|
ENSP00000425670.1:p.Thr478=
|
|
|
ENST00000508579.5:c.795G>T
(CAST)
|
ENSP00000425787.1:p.Thr265=
|
|
|
ENST00000508608.5:c.1788G>T
(CAST)
|
ENSP00000422677.1:p.Thr596=
|
|
|
ENST00000508830.5:c.1899G>T
(CAST)
|
ENSP00000425721.1:p.Thr633=
|
|
|
ENST00000509903.5:c.1545G>T
(CAST)
|
ENSP00000426946.1:p.Thr515=
|
|
|
ENST00000510098.1:c.135G>T
(CAST)
|
ENSP00000427195.1:p.Thr45=
|
|
|
ENST00000510156.5:c.1650G>T
(CAST)
|
ENSP00000422325.1:p.Thr550=
|
|
|
ENST00000510500.5:c.922G>T
(CAST)
|
|
|
|
ENST00000510756.5:c.1833G>T
(CAST)
|
ENSP00000422176.1:p.Thr611=
|
|
|
ENST00000511049.5:c.1608G>T
(CAST)
|
ENSP00000421130.1:p.Thr536=
|
|
|
ENST00000511782.5:c.1608G>T
(CAST)
|
ENSP00000423638.1:p.Thr536=
|
|
|
ENST00000515663.5:c.819G>T
(CAST)
|
ENSP00000422929.1:p.Thr273=
|
|
|
NM_001042440.3:c.1776G>T
(CAST)
|
NP_001035905.1:p.Thr592=
|
|
|
NM_001190442.1:c.1611G>T
(CAST)
|
NP_001177371.1:p.Thr537=
|
|
|
NM_001284212.1:c.1527G>T
(CAST)
|
NP_001271141.1:p.Thr509=
|
|
|
NM_001284213.1:c.1434G>T
(CAST)
|
NP_001271142.1:p.Thr478=
|
|
|
NM_016442.3:c.*861C>A
(ERAP1)
|
NP_057526.3:n.*861C>A
|
|
|
NM_173060.3:c.1584G>T
(CAST)
|
NP_775083.1:p.Thr528=
|
|
|
NR_104285.1:n.906G>T
(CAST)
|
|
|
|
XM_006714696.2:c.1899G>T
(CAST)
|
XP_006714759.1:p.Thr633=
|
|
|
XM_006714697.2:c.1899G>T
(CAST)
|
XP_006714760.1:p.Thr633=
|
|
|
XM_006714698.2:c.1860G>T
(CAST)
|
XP_006714761.1:p.Thr620=
|
|
|
XM_006714699.2:c.1854G>T
(CAST)
|
XP_006714762.1:p.Thr618=
|
|
|
XM_006714700.2:c.1842G>T
(CAST)
|
XP_006714763.1:p.Thr614=
|
|
|
XM_006714701.2:c.1833G>T
(CAST)
|
XP_006714764.1:p.Thr611=
|
|
|
XM_006714702.2:c.1797G>T
(CAST)
|
XP_006714765.1:p.Thr599=
|
|
|
XM_006714703.2:c.1794G>T
(CAST)
|
XP_006714766.1:p.Thr598=
|
|
|
XM_006714704.2:c.1788G>T
(CAST)
|
XP_006714767.1:p.Thr596=
|
|
|
XM_006714705.2:c.1776G>T
(CAST)
|
XP_006714768.1:p.Thr592=
|
|
|
XM_006714706.2:c.1731G>T
(CAST)
|
XP_006714769.1:p.Thr577=
|
|
|
XM_006714707.2:c.1650G>T
(CAST)
|
XP_006714770.1:p.Thr550=
|
|
|
XM_006714708.2:c.1611G>T
(CAST)
|
XP_006714771.1:p.Thr537=
|
|
|
XM_006714709.2:c.1593G>T
(CAST)
|
XP_006714772.1:p.Thr531=
|
|
|
XM_006714710.2:c.1545G>T
(CAST)
|
XP_006714773.1:p.Thr515=
|
|
|
XM_006714711.2:c.1527G>T
(CAST)
|
XP_006714774.1:p.Thr509=
|
|
|
XM_006714712.2:c.1488G>T
(CAST)
|
XP_006714775.1:p.Thr496=
|
|
|
XM_006714713.2:c.819G>T
(CAST)
|
XP_006714776.1:p.Thr273=
|
|
|
XM_006714714.2:c.819G>T
(CAST)
|
XP_006714777.1:p.Thr273=
|
|
|
XM_006714715.2:c.795G>T
(CAST)
|
XP_006714778.1:p.Thr265=
|
|
|
XM_011543487.1:c.*861C>A
(ERAP1)
|
XP_011541789.1:n.*861C>A
|
|
|
XM_011543654.1:c.1818G>T
(CAST)
|
XP_011541956.1:p.Thr606=
|
|
|
XM_011543655.1:c.1815G>T
(CAST)
|
XP_011541957.1:p.Thr605=
|
|
|
XM_011543656.1:c.1752G>T
(CAST)
|
XP_011541958.1:p.Thr584=
|
|
|
XM_011543657.1:c.1707G>T
(CAST)
|
XP_011541959.1:p.Thr569=
|
|
|
XM_011543658.1:c.1503G>T
(CAST)
|
XP_011541960.1:p.Thr501=
|
|
|
NM_001042440.4:c.1776G>T
(CAST)
|
NP_001035905.1:p.Thr592=
|
|
|
NM_001042441.2:c.1842G>T
(CAST)
|
NP_001035906.1:p.Thr614=
|
|
|
NM_001042442.2:c.1833G>T
(CAST)
|
NP_001035907.1:p.Thr611=
|
|
|
NM_001042443.2:c.1650G>T
(CAST)
|
NP_001035908.1:p.Thr550=
|
|
|
NM_001042444.2:c.1527G>T
(CAST)
|
NP_001035909.1:p.Thr509=
|
|
|
NM_001042445.2:c.1545G>T
(CAST)
|
NP_001035910.1:p.Thr515=
|
|
|
NM_001042446.2:c.1488G>T
(CAST)
|
NP_001035911.1:p.Thr496=
|
|
|
NM_001284212.3:c.1527G>T
(CAST)
|
NP_001271141.1:p.Thr509=
|
|
|
NM_001284213.3:c.1434G>T
(CAST)
|
NP_001271142.1:p.Thr478=
|
|
|
NM_001330626.1:c.1803G>T
(CAST)
|
NP_001317555.1:p.Thr601=
|
|
|
NM_001330627.1:c.1776G>T
(CAST)
|
NP_001317556.1:p.Thr592=
|
|
|
NM_001330628.1:c.1731G>T
(CAST)
|
NP_001317557.1:p.Thr577=
|
|
|
NM_001330629.1:c.1815G>T
(CAST)
|
NP_001317558.1:p.Thr605=
|
|
|
NM_001330630.1:c.1488G>T
(CAST)
|
NP_001317559.1:p.Thr496=
|
|
|
NM_001330631.1:c.1611G>T
(CAST)
|
NP_001317560.1:p.Thr537=
|
|
|
NM_001330632.1:c.1584G>T
(CAST)
|
NP_001317561.1:p.Thr528=
|
|
|
NM_001330633.1:c.1593G>T
(CAST)
|
NP_001317562.1:p.Thr531=
|
|
|
NM_001330634.1:c.1554G>T
(CAST)
|
NP_001317563.1:p.Thr518=
|
|
|
NM_001349244.1:c.*861C>A
(ERAP1)
|
NP_001336173.1:n.*861C>A
|
|
|
NM_001750.6:c.1899G>T
(CAST)
|
NP_001741.4:p.Thr633=
|
|
|
NM_016442.4:c.*861C>A
(ERAP1)
|
NP_057526.3:n.*861C>A
|
|
|
NM_173060.4:c.1584G>T
(CAST)
|
NP_775083.1:p.Thr528=
|
|
|
XR_001742119.2:n.3846C>A
(ERAP1)
|
|
|
|
NM_001042440.5:c.1776G>T
(CAST)
|
NP_001035905.1:p.Thr592=
|
|
|
NM_001042441.3:c.1842G>T
(CAST)
|
NP_001035906.1:p.Thr614=
|
|
|
NM_001042442.3:c.1833G>T
(CAST)
|
NP_001035907.1:p.Thr611=
|
|
|
NM_001330626.2:c.1803G>T
(CAST)
|
NP_001317555.1:p.Thr601=
|
|
|
NM_001330627.2:c.1776G>T
(CAST)
|
NP_001317556.1:p.Thr592=
|
|
|
NM_001330628.2:c.1731G>T
(CAST)
|
NP_001317557.1:p.Thr577=
|
|
|
NM_001330629.2:c.1815G>T
(CAST)
|
NP_001317558.1:p.Thr605=
|
|
|
NM_001375317.1:c.1788G>T
(CAST)
|
NP_001362246.1:p.Thr596=
|
|
|
NM_001750.7:c.1899G>T
(CAST)
MANE Select
|
NP_001741.4:p.Thr633=
|
|
|
NR_104285.2:n.844G>T
(CAST)
|
|
|
|
NM_001042443.3:c.1650G>T
(CAST)
|
NP_001035908.1:p.Thr550=
|
|
|
NM_001042444.3:c.1527G>T
(CAST)
|
NP_001035909.1:p.Thr509=
|
|
|
NM_001042445.3:c.1545G>T
(CAST)
|
NP_001035910.1:p.Thr515=
|
|
|
NM_001042446.3:c.1488G>T
(CAST)
|
NP_001035911.1:p.Thr496=
|
|
|
NM_001190442.2:c.1611G>T
(CAST)
|
NP_001177371.1:p.Thr537=
|
|
|
NM_001284212.4:c.1527G>T
(CAST)
|
NP_001271141.1:p.Thr509=
|
|
|
NM_001284213.4:c.1434G>T
(CAST)
|
NP_001271142.1:p.Thr478=
|
|
|
NM_001330630.2:c.1488G>T
(CAST)
|
NP_001317559.1:p.Thr496=
|
|
|
NM_001330631.2:c.1611G>T
(CAST)
|
NP_001317560.1:p.Thr537=
|
|
|
NM_001330632.2:c.1584G>T
(CAST)
|
NP_001317561.1:p.Thr528=
|
|
|
NM_001330633.2:c.1593G>T
(CAST)
|
NP_001317562.1:p.Thr531=
|
|
|
NM_001330634.2:c.1554G>T
(CAST)
|
NP_001317563.1:p.Thr518=
|
|
|
NM_001349244.2:c.*861C>A
(ERAP1)
|
NP_001336173.1:n.*861C>A
|
|
|
NM_016442.5:c.*861C>A
(ERAP1)
|
NP_057526.3:n.*861C>A
|
|
|
NM_173060.5:c.1584G>T
(CAST)
|
NP_775083.1:p.Thr528=
|
|
