|
ENST00000484552.6:c.820A>T
(CAST)
|
ENSP00000432878.2:p.Thr274Ser
|
|
|
ENST00000508608.6:c.1750A>T
(CAST)
|
ENSP00000422677.2:p.Thr584Ser
|
|
|
ENST00000510756.6:c.1528A>T
(CAST)
|
ENSP00000422176.2:p.Thr510Ser
|
|
|
ENST00000674587.1:c.1357A>T
(CAST)
|
ENSP00000501797.1:p.Thr453Ser
|
|
|
ENST00000674702.1:c.1642A>T
(CAST)
|
ENSP00000502345.1:p.Thr548Ser
|
|
|
ENST00000674984.1:c.1834A>T
(CAST)
|
ENSP00000501713.1:p.Thr612Ser
|
|
|
ENST00000675033.1:c.1528A>T
(CAST)
|
ENSP00000501659.1:p.Thr510Ser
|
|
|
ENST00000675179.1:c.1900A>T
(CAST)
MANE Select
|
ENSP00000501872.1:p.Thr634Ser
|
|
|
ENST00000675185.1:c.281A>T
(CAST)
|
|
|
|
ENST00000675266.1:c.1802A>T
(CAST)
|
|
|
|
ENST00000675267.1:c.*1524A>T
(CAST)
|
ENSP00000502095.1:n.*1524A>T
|
|
|
ENST00000675275.1:c.617A>T
(CAST)
|
|
|
|
ENST00000675479.1:c.1513A>T
(CAST)
|
ENSP00000502244.1:p.Thr505Ser
|
|
|
ENST00000675614.1:c.1570A>T
(CAST)
|
ENSP00000502136.1:p.Thr524Ser
|
|
|
ENST00000675663.1:c.1789A>T
(CAST)
|
ENSP00000502449.1:p.Thr597Ser
|
|
|
ENST00000675734.1:n.444A>T
(CAST)
|
|
|
|
ENST00000675858.1:c.1444A>T
(CAST)
|
ENSP00000501780.1:p.Thr482Ser
|
|
|
ENST00000296754.7:c.*860T>A
(ERAP1)
|
ENSP00000296754.3:n.*860T>A
|
|
|
ENST00000309190.9:c.1585A>T
(CAST)
|
ENSP00000312523.5:p.Thr529Ser
|
|
|
ENST00000325674.11:c.820A>T
(CAST)
|
ENSP00000320319.8:p.Thr274Ser
|
|
|
ENST00000338252.7:c.1612A>T
(CAST)
|
ENSP00000343421.3:p.Thr538Ser
|
|
|
ENST00000341926.7:c.1651A>T
(CAST)
|
ENSP00000339914.3:p.Thr551Ser
|
|
|
ENST00000348386.7:n.1593A>T
(CAST)
|
|
|
|
ENST00000395812.6:c.1777A>T
(CAST)
|
ENSP00000379157.2:p.Thr593Ser
|
|
|
ENST00000395813.5:c.1651A>T
(CAST)
|
ENSP00000379158.2:p.Thr551Ser
|
|
|
ENST00000437034.6:c.906A>T
(CAST)
|
|
|
|
ENST00000484552.5:c.878A>T
(CAST)
|
|
|
|
ENST00000504465.5:c.1435A>T
(CAST)
|
ENSP00000425670.1:p.Thr479Ser
|
|
|
ENST00000508579.5:c.796A>T
(CAST)
|
ENSP00000425787.1:p.Thr266Ser
|
|
|
ENST00000508608.5:c.1789A>T
(CAST)
|
ENSP00000422677.1:p.Thr597Ser
|
|
|
ENST00000508830.5:c.1900A>T
(CAST)
|
ENSP00000425721.1:p.Thr634Ser
|
|
|
ENST00000509903.5:c.1546A>T
(CAST)
|
ENSP00000426946.1:p.Thr516Ser
|
|
|
ENST00000510098.1:c.136A>T
(CAST)
|
ENSP00000427195.1:p.Thr46Ser
|
|
|
ENST00000510156.5:c.1651A>T
(CAST)
|
ENSP00000422325.1:p.Thr551Ser
|
|
|
ENST00000510500.5:c.923A>T
(CAST)
|
|
|
|
ENST00000510756.5:c.1834A>T
(CAST)
|
ENSP00000422176.1:p.Thr612Ser
|
|
|
ENST00000511049.5:c.1609A>T
(CAST)
|
ENSP00000421130.1:p.Thr537Ser
|
|
|
ENST00000511782.5:c.1609A>T
(CAST)
|
ENSP00000423638.1:p.Thr537Ser
|
|
|
ENST00000515663.5:c.820A>T
(CAST)
|
ENSP00000422929.1:p.Thr274Ser
|
|
|
NM_001042440.3:c.1777A>T
(CAST)
|
NP_001035905.1:p.Thr593Ser
|
|
|
NM_001190442.1:c.1612A>T
(CAST)
|
NP_001177371.1:p.Thr538Ser
|
|
|
NM_001284212.1:c.1528A>T
(CAST)
|
NP_001271141.1:p.Thr510Ser
|
|
|
NM_001284213.1:c.1435A>T
(CAST)
|
NP_001271142.1:p.Thr479Ser
|
|
|
NM_016442.3:c.*860T>A
(ERAP1)
|
NP_057526.3:n.*860T>A
|
|
|
NM_173060.3:c.1585A>T
(CAST)
|
NP_775083.1:p.Thr529Ser
|
|
|
NR_104285.1:n.907A>T
(CAST)
|
|
|
|
XM_006714696.2:c.1900A>T
(CAST)
|
XP_006714759.1:p.Thr634Ser
|
|
|
XM_006714697.2:c.1900A>T
(CAST)
|
XP_006714760.1:p.Thr634Ser
|
|
|
XM_006714698.2:c.1861A>T
(CAST)
|
XP_006714761.1:p.Thr621Ser
|
|
|
XM_006714699.2:c.1855A>T
(CAST)
|
XP_006714762.1:p.Thr619Ser
|
|
|
XM_006714700.2:c.1843A>T
(CAST)
|
XP_006714763.1:p.Thr615Ser
|
|
|
XM_006714701.2:c.1834A>T
(CAST)
|
XP_006714764.1:p.Thr612Ser
|
|
|
XM_006714702.2:c.1798A>T
(CAST)
|
XP_006714765.1:p.Thr600Ser
|
|
|
XM_006714703.2:c.1795A>T
(CAST)
|
XP_006714766.1:p.Thr599Ser
|
|
|
XM_006714704.2:c.1789A>T
(CAST)
|
XP_006714767.1:p.Thr597Ser
|
|
|
XM_006714705.2:c.1777A>T
(CAST)
|
XP_006714768.1:p.Thr593Ser
|
|
|
XM_006714706.2:c.1732A>T
(CAST)
|
XP_006714769.1:p.Thr578Ser
|
|
|
XM_006714707.2:c.1651A>T
(CAST)
|
XP_006714770.1:p.Thr551Ser
|
|
|
XM_006714708.2:c.1612A>T
(CAST)
|
XP_006714771.1:p.Thr538Ser
|
|
|
XM_006714709.2:c.1594A>T
(CAST)
|
XP_006714772.1:p.Thr532Ser
|
|
|
XM_006714710.2:c.1546A>T
(CAST)
|
XP_006714773.1:p.Thr516Ser
|
|
|
XM_006714711.2:c.1528A>T
(CAST)
|
XP_006714774.1:p.Thr510Ser
|
|
|
XM_006714712.2:c.1489A>T
(CAST)
|
XP_006714775.1:p.Thr497Ser
|
|
|
XM_006714713.2:c.820A>T
(CAST)
|
XP_006714776.1:p.Thr274Ser
|
|
|
XM_006714714.2:c.820A>T
(CAST)
|
XP_006714777.1:p.Thr274Ser
|
|
|
XM_006714715.2:c.796A>T
(CAST)
|
XP_006714778.1:p.Thr266Ser
|
|
|
XM_011543487.1:c.*860T>A
(ERAP1)
|
XP_011541789.1:n.*860T>A
|
|
|
XM_011543654.1:c.1819A>T
(CAST)
|
XP_011541956.1:p.Thr607Ser
|
|
|
XM_011543655.1:c.1816A>T
(CAST)
|
XP_011541957.1:p.Thr606Ser
|
|
|
XM_011543656.1:c.1753A>T
(CAST)
|
XP_011541958.1:p.Thr585Ser
|
|
|
XM_011543657.1:c.1708A>T
(CAST)
|
XP_011541959.1:p.Thr570Ser
|
|
|
XM_011543658.1:c.1504A>T
(CAST)
|
XP_011541960.1:p.Thr502Ser
|
|
|
NM_001042440.4:c.1777A>T
(CAST)
|
NP_001035905.1:p.Thr593Ser
|
|
|
NM_001042441.2:c.1843A>T
(CAST)
|
NP_001035906.1:p.Thr615Ser
|
|
|
NM_001042442.2:c.1834A>T
(CAST)
|
NP_001035907.1:p.Thr612Ser
|
|
|
NM_001042443.2:c.1651A>T
(CAST)
|
NP_001035908.1:p.Thr551Ser
|
|
|
NM_001042444.2:c.1528A>T
(CAST)
|
NP_001035909.1:p.Thr510Ser
|
|
|
NM_001042445.2:c.1546A>T
(CAST)
|
NP_001035910.1:p.Thr516Ser
|
|
|
NM_001042446.2:c.1489A>T
(CAST)
|
NP_001035911.1:p.Thr497Ser
|
|
|
NM_001284212.3:c.1528A>T
(CAST)
|
NP_001271141.1:p.Thr510Ser
|
|
|
NM_001284213.3:c.1435A>T
(CAST)
|
NP_001271142.1:p.Thr479Ser
|
|
|
NM_001330626.1:c.1804A>T
(CAST)
|
NP_001317555.1:p.Thr602Ser
|
|
|
NM_001330627.1:c.1777A>T
(CAST)
|
NP_001317556.1:p.Thr593Ser
|
|
|
NM_001330628.1:c.1732A>T
(CAST)
|
NP_001317557.1:p.Thr578Ser
|
|
|
NM_001330629.1:c.1816A>T
(CAST)
|
NP_001317558.1:p.Thr606Ser
|
|
|
NM_001330630.1:c.1489A>T
(CAST)
|
NP_001317559.1:p.Thr497Ser
|
|
|
NM_001330631.1:c.1612A>T
(CAST)
|
NP_001317560.1:p.Thr538Ser
|
|
|
NM_001330632.1:c.1585A>T
(CAST)
|
NP_001317561.1:p.Thr529Ser
|
|
|
NM_001330633.1:c.1594A>T
(CAST)
|
NP_001317562.1:p.Thr532Ser
|
|
|
NM_001330634.1:c.1555A>T
(CAST)
|
NP_001317563.1:p.Thr519Ser
|
|
|
NM_001349244.1:c.*860T>A
(ERAP1)
|
NP_001336173.1:n.*860T>A
|
|
|
NM_001750.6:c.1900A>T
(CAST)
|
NP_001741.4:p.Thr634Ser
|
|
|
NM_016442.4:c.*860T>A
(ERAP1)
|
NP_057526.3:n.*860T>A
|
|
|
NM_173060.4:c.1585A>T
(CAST)
|
NP_775083.1:p.Thr529Ser
|
|
|
XR_001742119.2:n.3845T>A
(ERAP1)
|
|
|
|
NM_001042440.5:c.1777A>T
(CAST)
|
NP_001035905.1:p.Thr593Ser
|
|
|
NM_001042441.3:c.1843A>T
(CAST)
|
NP_001035906.1:p.Thr615Ser
|
|
|
NM_001042442.3:c.1834A>T
(CAST)
|
NP_001035907.1:p.Thr612Ser
|
|
|
NM_001330626.2:c.1804A>T
(CAST)
|
NP_001317555.1:p.Thr602Ser
|
|
|
NM_001330627.2:c.1777A>T
(CAST)
|
NP_001317556.1:p.Thr593Ser
|
|
|
NM_001330628.2:c.1732A>T
(CAST)
|
NP_001317557.1:p.Thr578Ser
|
|
|
NM_001330629.2:c.1816A>T
(CAST)
|
NP_001317558.1:p.Thr606Ser
|
|
|
NM_001375317.1:c.1789A>T
(CAST)
|
NP_001362246.1:p.Thr597Ser
|
|
|
NM_001750.7:c.1900A>T
(CAST)
MANE Select
|
NP_001741.4:p.Thr634Ser
|
|
|
NR_104285.2:n.845A>T
(CAST)
|
|
|
|
NM_001042443.3:c.1651A>T
(CAST)
|
NP_001035908.1:p.Thr551Ser
|
|
|
NM_001042444.3:c.1528A>T
(CAST)
|
NP_001035909.1:p.Thr510Ser
|
|
|
NM_001042445.3:c.1546A>T
(CAST)
|
NP_001035910.1:p.Thr516Ser
|
|
|
NM_001042446.3:c.1489A>T
(CAST)
|
NP_001035911.1:p.Thr497Ser
|
|
|
NM_001190442.2:c.1612A>T
(CAST)
|
NP_001177371.1:p.Thr538Ser
|
|
|
NM_001284212.4:c.1528A>T
(CAST)
|
NP_001271141.1:p.Thr510Ser
|
|
|
NM_001284213.4:c.1435A>T
(CAST)
|
NP_001271142.1:p.Thr479Ser
|
|
|
NM_001330630.2:c.1489A>T
(CAST)
|
NP_001317559.1:p.Thr497Ser
|
|
|
NM_001330631.2:c.1612A>T
(CAST)
|
NP_001317560.1:p.Thr538Ser
|
|
|
NM_001330632.2:c.1585A>T
(CAST)
|
NP_001317561.1:p.Thr529Ser
|
|
|
NM_001330633.2:c.1594A>T
(CAST)
|
NP_001317562.1:p.Thr532Ser
|
|
|
NM_001330634.2:c.1555A>T
(CAST)
|
NP_001317563.1:p.Thr519Ser
|
|
|
NM_001349244.2:c.*860T>A
(ERAP1)
|
NP_001336173.1:n.*860T>A
|
|
|
NM_016442.5:c.*860T>A
(ERAP1)
|
NP_057526.3:n.*860T>A
|
|
|
NM_173060.5:c.1585A>T
(CAST)
|
NP_775083.1:p.Thr529Ser
|
|
