ENST00000262304.9:c.11187C>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.His3729=
|
|
ENST00000262304.8:c.11187C>T
(PKD1)
|
ENSP00000262304.4:p.His3729=
|
|
ENST00000423118.5:c.11184C>T
(PKD1)
|
ENSP00000399501.1:p.His3728=
|
|
ENST00000485120.1:n.36C>T
(PKD1)
|
|
|
ENST00000487932.5:c.5749C>T
(PKD1)
|
ENSP00000457132.1:n.5749C>T
|
|
ENST00000562425.1:c.300C>T
(PKD1)
|
|
|
ENST00000567355.1:n.350C>T
(PKD1)
|
|
|
NM_000296.3:c.11184C>T
(PKD1)
|
NP_000287.3:p.His3728=
|
|
NM_001009944.2:c.11187C>T
(PKD1)
|
NP_001009944.2:p.His3729=
|
|
XM_005255370.2:c.8142C>T
(PKD1)
|
XP_005255427.1:p.His2714=
|
|
XM_011522525.1:c.11265C>T
(PKD1)
|
XP_011520827.1:p.His3755=
|
|
XM_011522526.1:c.11262C>T
(PKD1)
|
XP_011520828.1:p.His3754=
|
|
XM_011522527.1:c.11247C>T
(PKD1)
|
XP_011520829.1:p.His3749=
|
|
XM_011522528.1:c.11241C>T
(PKD1)
|
XP_011520830.1:p.His3747=
|
|
XM_011522529.1:c.11238C>T
(PKD1)
|
XP_011520831.1:p.His3746=
|
|
XM_011522530.1:c.11211C>T
(PKD1)
|
XP_011520832.1:p.His3737=
|
|
XM_011522531.1:c.11193C>T
(PKD1)
|
XP_011520833.1:p.His3731=
|
|
XM_011522532.1:c.11139C>T
(PKD1)
|
XP_011520834.1:p.His3713=
|
|
XM_011522533.1:c.11058C>T
(PKD1)
|
XP_011520835.1:p.His3686=
|
|
XM_011522534.1:c.11001C>T
(PKD1)
|
XP_011520836.1:p.His3667=
|
|
XM_011522535.1:c.9087C>T
(PKD1)
|
XP_011520837.1:p.His3029=
|
|
XM_011522537.1:c.8265C>T
(PKD1)
|
XP_011520839.1:p.His2755=
|
|
XR_932867.1:n.11280C>T
(PKD1)
|
|
|
XR_932868.1:n.11110-374C>T
(PKD1)
|
|
|
XR_932869.1:n.11110-374C>T
(PKD1)
|
|
|
XR_932870.1:n.11140C>T
(PKD1)
|
|
|
XR_933000.1:n.90-327G>A
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-327G>A
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-327G>A
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-327G>A
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-327G>A
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8142C>T
(PKD1)
|
XP_005255427.1:p.His2714=
|
|
XM_011522528.3:c.11241C>T
(PKD1)
|
XP_011520830.1:p.His3747=
|
|
XM_011522529.2:c.11238C>T
(PKD1)
|
XP_011520831.1:p.His3746=
|
|
XM_011522537.2:c.8265C>T
(PKD1)
|
XP_011520839.1:p.His2755=
|
|
XM_024450298.1:c.11307C>T
(PKD1)
|
XP_024306066.1:p.His3769=
|
|
XM_024450299.1:c.11235C>T
(PKD1)
|
XP_024306067.1:p.His3745=
|
|
XM_024450300.1:c.11097C>T
(PKD1)
|
XP_024306068.1:p.His3699=
|
|
XM_024450301.1:c.9183C>T
(PKD1)
|
XP_024306069.1:p.His3061=
|
|
NM_000296.4:c.11184C>T
(PKD1)
|
NP_000287.4:p.His3728=
|
|
NM_001009944.3:c.11187C>T
(PKD1)
MANE Select
|
NP_001009944.3:p.His3729=
|
|