|
ENST00000262304.9:c.11157G>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Arg3719=
|
|
|
ENST00000262304.8:c.11157G>T
(PKD1)
|
ENSP00000262304.4:p.Arg3719=
|
|
|
ENST00000423118.5:c.11154G>T
(PKD1)
|
ENSP00000399501.1:p.Arg3718=
|
|
|
ENST00000485120.1:n.6G>T
(PKD1)
|
|
|
|
ENST00000487932.5:c.5719G>T
(PKD1)
|
ENSP00000457132.1:n.5719G>T
|
|
|
ENST00000562425.1:c.270G>T
(PKD1)
|
|
|
|
ENST00000567355.1:n.320G>T
(PKD1)
|
|
|
|
NM_000296.3:c.11154G>T
(PKD1)
|
NP_000287.3:p.Arg3718=
|
|
|
NM_001009944.2:c.11157G>T
(PKD1)
|
NP_001009944.2:p.Arg3719=
|
|
|
XM_005255370.2:c.8112G>T
(PKD1)
|
XP_005255427.1:p.Arg2704=
|
|
|
XM_011522525.1:c.11235G>T
(PKD1)
|
XP_011520827.1:p.Arg3745=
|
|
|
XM_011522526.1:c.11232G>T
(PKD1)
|
XP_011520828.1:p.Arg3744=
|
|
|
XM_011522527.1:c.11217G>T
(PKD1)
|
XP_011520829.1:p.Arg3739=
|
|
|
XM_011522528.1:c.11211G>T
(PKD1)
|
XP_011520830.1:p.Arg3737=
|
|
|
XM_011522529.1:c.11208G>T
(PKD1)
|
XP_011520831.1:p.Arg3736=
|
|
|
XM_011522530.1:c.11181G>T
(PKD1)
|
XP_011520832.1:p.Arg3727=
|
|
|
XM_011522531.1:c.11163G>T
(PKD1)
|
XP_011520833.1:p.Arg3721=
|
|
|
XM_011522532.1:c.11109G>T
(PKD1)
|
XP_011520834.1:p.Arg3703=
|
|
|
XM_011522533.1:c.11028G>T
(PKD1)
|
XP_011520835.1:p.Arg3676=
|
|
|
XM_011522534.1:c.10971G>T
(PKD1)
|
XP_011520836.1:p.Arg3657=
|
|
|
XM_011522535.1:c.9057G>T
(PKD1)
|
XP_011520837.1:p.Arg3019=
|
|
|
XM_011522537.1:c.8235G>T
(PKD1)
|
XP_011520839.1:p.Arg2745=
|
|
|
XR_932867.1:n.11250G>T
(PKD1)
|
|
|
|
XR_932868.1:n.11110-404G>T
(PKD1)
|
|
|
|
XR_932869.1:n.11110-404G>T
(PKD1)
|
|
|
|
XR_932870.1:n.11110G>T
(PKD1)
|
|
|
|
XR_933000.1:n.90-297C>A
(PKD1-AS1)
|
|
|
|
XR_933001.1:n.180-297C>A
(PKD1-AS1)
|
|
|
|
XR_933002.1:n.89-297C>A
(PKD1-AS1)
|
|
|
|
XR_933003.1:n.89-297C>A
(PKD1-AS1)
|
|
|
|
NR_135175.1:n.180-297C>A
(PKD1-AS1)
|
|
|
|
XM_005255370.3:c.8112G>T
(PKD1)
|
XP_005255427.1:p.Arg2704=
|
|
|
XM_011522528.3:c.11211G>T
(PKD1)
|
XP_011520830.1:p.Arg3737=
|
|
|
XM_011522529.2:c.11208G>T
(PKD1)
|
XP_011520831.1:p.Arg3736=
|
|
|
XM_011522537.2:c.8235G>T
(PKD1)
|
XP_011520839.1:p.Arg2745=
|
|
|
XM_024450298.1:c.11277G>T
(PKD1)
|
XP_024306066.1:p.Arg3759=
|
|
|
XM_024450299.1:c.11205G>T
(PKD1)
|
XP_024306067.1:p.Arg3735=
|
|
|
XM_024450300.1:c.11067G>T
(PKD1)
|
XP_024306068.1:p.Arg3689=
|
|
|
XM_024450301.1:c.9153G>T
(PKD1)
|
XP_024306069.1:p.Arg3051=
|
|
|
NM_000296.4:c.11154G>T
(PKD1)
|
NP_000287.4:p.Arg3718=
|
|
|
NM_001009944.3:c.11157G>T
(PKD1)
MANE Select
|
NP_001009944.3:p.Arg3719=
|
|
