ENST00000262304.9:c.7217C>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Ala2406Val
|
|
ENST00000262304.8:c.7217C>T
(PKD1)
|
ENSP00000262304.4:p.Ala2406Val
|
|
ENST00000415938.7:n.462C>T
(PKD1)
|
|
|
ENST00000423118.5:c.7217C>T
(PKD1)
|
ENSP00000399501.1:p.Ala2406Val
|
|
ENST00000483024.1:c.385C>T
(PKD1)
|
|
|
ENST00000483558.5:n.276C>T
(PKD1)
|
|
|
ENST00000483731.5:n.942C>T
(PKD1)
|
|
|
ENST00000486339.6:n.963C>T
(PKD1)
|
|
|
ENST00000487932.5:c.1904C>T
(PKD1)
|
ENSP00000457132.1:p.Ala635Val
|
|
ENST00000496574.6:n.1220C>T
(PKD1)
|
|
|
ENST00000565639.6:n.925C>T
(PKD1)
|
|
|
ENST00000568591.5:c.2378C>T
(PKD1)
|
ENSP00000457162.1:n.2378C>T
|
|
ENST00000569983.5:n.573C>T
(PKD1)
|
|
|
NM_000296.3:c.7217C>T
(PKD1)
|
NP_000287.3:p.Ala2406Val
|
|
NM_001009944.2:c.7217C>T
(PKD1)
|
NP_001009944.2:p.Ala2406Val
|
|
NR_106775.1:n.84C>T
(MIR6511B1)
|
|
|
XM_005255370.2:c.4172C>T
(PKD1)
|
XP_005255427.1:p.Ala1391Val
|
|
XM_011522525.1:c.7295C>T
(PKD1)
|
XP_011520827.1:p.Ala2432Val
|
|
XM_011522526.1:c.7295C>T
(PKD1)
|
XP_011520828.1:p.Ala2432Val
|
|
XM_011522527.1:c.7295C>T
(PKD1)
|
XP_011520829.1:p.Ala2432Val
|
|
XM_011522528.1:c.7271C>T
(PKD1)
|
XP_011520830.1:p.Ala2424Val
|
|
XM_011522529.1:c.7271C>T
(PKD1)
|
XP_011520831.1:p.Ala2424Val
|
|
XM_011522530.1:c.7241C>T
(PKD1)
|
XP_011520832.1:p.Ala2414Val
|
|
XM_011522531.1:c.7223C>T
(PKD1)
|
XP_011520833.1:p.Ala2408Val
|
|
XM_011522532.1:c.7169C>T
(PKD1)
|
XP_011520834.1:p.Ala2390Val
|
|
XM_011522533.1:c.7088C>T
(PKD1)
|
XP_011520835.1:p.Ala2363Val
|
|
XM_011522534.1:c.7031C>T
(PKD1)
|
XP_011520836.1:p.Ala2344Val
|
|
XM_011522535.1:c.5117C>T
(PKD1)
|
XP_011520837.1:p.Ala1706Val
|
|
XM_011522536.1:c.7295C>T
(PKD1)
|
XP_011520838.1:p.Ala2432Val
|
|
XM_011522537.1:c.4295C>T
(PKD1)
|
XP_011520839.1:p.Ala1432Val
|
|
XR_932867.1:n.7310C>T
(PKD1)
|
|
|
XR_932868.1:n.7310C>T
(PKD1)
|
|
|
XR_932869.1:n.7310C>T
(PKD1)
|
|
|
XR_932870.1:n.7310C>T
(PKD1)
|
|
|
XM_005255370.3:c.4172C>T
(PKD1)
|
XP_005255427.1:p.Ala1391Val
|
|
XM_011522528.3:c.7271C>T
(PKD1)
|
XP_011520830.1:p.Ala2424Val
|
|
XM_011522529.2:c.7271C>T
(PKD1)
|
XP_011520831.1:p.Ala2424Val
|
|
XM_011522537.2:c.4295C>T
(PKD1)
|
XP_011520839.1:p.Ala1432Val
|
|
XM_024450298.1:c.7337C>T
(PKD1)
|
XP_024306066.1:p.Ala2446Val
|
|
XM_024450299.1:c.7265C>T
(PKD1)
|
XP_024306067.1:p.Ala2422Val
|
|
XM_024450300.1:c.7127C>T
(PKD1)
|
XP_024306068.1:p.Ala2376Val
|
|
XM_024450301.1:c.5213C>T
(PKD1)
|
XP_024306069.1:p.Ala1738Val
|
|
NM_000296.4:c.7217C>T
(PKD1)
|
NP_000287.4:p.Ala2406Val
|
|
NM_001009944.3:c.7217C>T
(PKD1)
MANE Select
|
NP_001009944.3:p.Ala2406Val
|
|