ENST00000262304.9:c.11235G>A
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Gly3745=
|
|
ENST00000262304.8:c.11235G>A
(PKD1)
|
ENSP00000262304.4:p.Gly3745=
|
|
ENST00000423118.5:c.11232G>A
(PKD1)
|
ENSP00000399501.1:p.Gly3744=
|
|
ENST00000485120.1:n.84G>A
(PKD1)
|
|
|
ENST00000487932.5:c.5797G>A
(PKD1)
|
ENSP00000457132.1:n.5797G>A
|
|
ENST00000562425.1:c.348G>A
(PKD1)
|
|
|
ENST00000567355.1:n.398G>A
(PKD1)
|
|
|
NM_000296.3:c.11232G>A
(PKD1)
|
NP_000287.3:p.Gly3744=
|
|
NM_001009944.2:c.11235G>A
(PKD1)
|
NP_001009944.2:p.Gly3745=
|
|
XM_005255370.2:c.8190G>A
(PKD1)
|
XP_005255427.1:p.Gly2730=
|
|
XM_011522525.1:c.11313G>A
(PKD1)
|
XP_011520827.1:p.Gly3771=
|
|
XM_011522526.1:c.11310G>A
(PKD1)
|
XP_011520828.1:p.Gly3770=
|
|
XM_011522527.1:c.11295G>A
(PKD1)
|
XP_011520829.1:p.Gly3765=
|
|
XM_011522528.1:c.11289G>A
(PKD1)
|
XP_011520830.1:p.Gly3763=
|
|
XM_011522529.1:c.11286G>A
(PKD1)
|
XP_011520831.1:p.Gly3762=
|
|
XM_011522530.1:c.11259G>A
(PKD1)
|
XP_011520832.1:p.Gly3753=
|
|
XM_011522531.1:c.11241G>A
(PKD1)
|
XP_011520833.1:p.Gly3747=
|
|
XM_011522532.1:c.11187G>A
(PKD1)
|
XP_011520834.1:p.Gly3729=
|
|
XM_011522533.1:c.11106G>A
(PKD1)
|
XP_011520835.1:p.Gly3702=
|
|
XM_011522534.1:c.11049G>A
(PKD1)
|
XP_011520836.1:p.Gly3683=
|
|
XM_011522535.1:c.9135G>A
(PKD1)
|
XP_011520837.1:p.Gly3045=
|
|
XM_011522537.1:c.8313G>A
(PKD1)
|
XP_011520839.1:p.Gly2771=
|
|
XR_932867.1:n.11328G>A
(PKD1)
|
|
|
XR_932868.1:n.11110-326G>A
(PKD1)
|
|
|
XR_932869.1:n.11110-326G>A
(PKD1)
|
|
|
XR_932870.1:n.11188G>A
(PKD1)
|
|
|
XR_933000.1:n.90-375C>T
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-375C>T
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-375C>T
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-375C>T
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-375C>T
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8190G>A
(PKD1)
|
XP_005255427.1:p.Gly2730=
|
|
XM_011522528.3:c.11289G>A
(PKD1)
|
XP_011520830.1:p.Gly3763=
|
|
XM_011522529.2:c.11286G>A
(PKD1)
|
XP_011520831.1:p.Gly3762=
|
|
XM_011522537.2:c.8313G>A
(PKD1)
|
XP_011520839.1:p.Gly2771=
|
|
XM_024450298.1:c.11355G>A
(PKD1)
|
XP_024306066.1:p.Gly3785=
|
|
XM_024450299.1:c.11283G>A
(PKD1)
|
XP_024306067.1:p.Gly3761=
|
|
XM_024450300.1:c.11145G>A
(PKD1)
|
XP_024306068.1:p.Gly3715=
|
|
XM_024450301.1:c.9231G>A
(PKD1)
|
XP_024306069.1:p.Gly3077=
|
|
NM_000296.4:c.11232G>A
(PKD1)
|
NP_000287.4:p.Gly3744=
|
|
NM_001009944.3:c.11235G>A
(PKD1)
MANE Select
|
NP_001009944.3:p.Gly3745=
|
|