|
NM_001009944.3:c.6877C>T
MANE Select
|
NP_001009944.3:p.Pro2293Ser
|
|
ENST00000262304.9:c.6877C>T
MANE Select
|
ENSP00000262304.4:p.Pro2293Ser
|
|
NM_000296.3:c.6877C>T
|
NP_000287.3:p.Pro2293Ser
|
|
NM_000296.4:c.6877C>T
|
NP_000287.4:p.Pro2293Ser
|
|
NM_001009944.2:c.6877C>T
|
NP_001009944.2:p.Pro2293Ser
|
|
ENST00000262304.8:c.6877C>T
|
ENSP00000262304.4:p.Pro2293Ser
|
|
ENST00000415938.7:n.311-1342C>T
|
|
|
ENST00000423118.5:c.6877C>T
|
ENSP00000399501.1:p.Pro2293Ser
|
|
ENST00000473780.2:n.259C>T
|
|
|
ENST00000483024.1:c.234-1342C>T
|
|
|
ENST00000483731.5:n.791-1342C>T
|
|
|
ENST00000487932.5:c.1564C>T
|
ENSP00000457132.1:p.Pro522Ser
|
|
ENST00000488185.2:c.541C>T
|
|
|
ENST00000565639.6:n.774-1342C>T
|
|
|
ENST00000568591.5:c.2227-1342C>T
|
ENSP00000457162.1:n.2227-1342C>T
|
|
ENST00000569983.5:n.422-1342C>T
|
|
|
XM_005255370.2:c.3832C>T
|
XP_005255427.1:p.Pro1278Ser
|
|
XM_005255370.3:c.3832C>T
|
XP_005255427.1:p.Pro1278Ser
|
|
XM_011522525.1:c.6955C>T
|
XP_011520827.1:p.Pro2319Ser
|
|
XM_011522526.1:c.6955C>T
|
XP_011520828.1:p.Pro2319Ser
|
|
XM_011522527.1:c.6955C>T
|
XP_011520829.1:p.Pro2319Ser
|
|
XM_011522528.1:c.6931C>T
|
XP_011520830.1:p.Pro2311Ser
|
|
XM_011522528.3:c.6931C>T
|
XP_011520830.1:p.Pro2311Ser
|
|
XM_011522529.1:c.6931C>T
|
XP_011520831.1:p.Pro2311Ser
|
|
XM_011522529.2:c.6931C>T
|
XP_011520831.1:p.Pro2311Ser
|
|
XM_011522530.1:c.6901C>T
|
XP_011520832.1:p.Pro2301Ser
|
|
XM_011522531.1:c.6883C>T
|
XP_011520833.1:p.Pro2295Ser
|
|
XM_011522532.1:c.6829C>T
|
XP_011520834.1:p.Pro2277Ser
|
|
XM_011522533.1:c.6748C>T
|
XP_011520835.1:p.Pro2250Ser
|
|
XM_011522534.1:c.6691C>T
|
XP_011520836.1:p.Pro2231Ser
|
|
XM_011522535.1:c.4777C>T
|
XP_011520837.1:p.Pro1593Ser
|
|
XM_011522536.1:c.6955C>T
|
XP_011520838.1:p.Pro2319Ser
|
|
XM_011522537.1:c.3955C>T
|
XP_011520839.1:p.Pro1319Ser
|
|
XM_011522537.2:c.3955C>T
|
XP_011520839.1:p.Pro1319Ser
|
|
XM_024450298.1:c.6997C>T
|
XP_024306066.1:p.Pro2333Ser
|
|
XM_024450299.1:c.6925C>T
|
XP_024306067.1:p.Pro2309Ser
|
|
XM_024450300.1:c.6787C>T
|
XP_024306068.1:p.Pro2263Ser
|
|
XM_024450301.1:c.4873C>T
|
XP_024306069.1:p.Pro1625Ser
|
|
XR_932867.1:n.6970C>T
|
|
|
XR_932868.1:n.6970C>T
|
|
|
XR_932869.1:n.6970C>T
|
|
|
XR_932870.1:n.6970C>T
|
|
