ENST00000262304.9:c.11260C>G
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Leu3754Val
|
|
ENST00000262304.8:c.11260C>G
(PKD1)
|
ENSP00000262304.4:p.Leu3754Val
|
|
ENST00000423118.5:c.11257C>G
(PKD1)
|
ENSP00000399501.1:p.Leu3753Val
|
|
ENST00000485120.1:n.109C>G
(PKD1)
|
|
|
ENST00000487932.5:c.5822C>G
(PKD1)
|
ENSP00000457132.1:n.5822C>G
|
|
ENST00000562425.1:c.373C>G
(PKD1)
|
|
|
ENST00000567355.1:n.423C>G
(PKD1)
|
|
|
NM_000296.3:c.11257C>G
(PKD1)
|
NP_000287.3:p.Leu3753Val
|
|
NM_001009944.2:c.11260C>G
(PKD1)
|
NP_001009944.2:p.Leu3754Val
|
|
XM_005255370.2:c.8215C>G
(PKD1)
|
XP_005255427.1:p.Leu2739Val
|
|
XM_011522525.1:c.11338C>G
(PKD1)
|
XP_011520827.1:p.Leu3780Val
|
|
XM_011522526.1:c.11335C>G
(PKD1)
|
XP_011520828.1:p.Leu3779Val
|
|
XM_011522527.1:c.11320C>G
(PKD1)
|
XP_011520829.1:p.Leu3774Val
|
|
XM_011522528.1:c.11314C>G
(PKD1)
|
XP_011520830.1:p.Leu3772Val
|
|
XM_011522529.1:c.11311C>G
(PKD1)
|
XP_011520831.1:p.Leu3771Val
|
|
XM_011522530.1:c.11284C>G
(PKD1)
|
XP_011520832.1:p.Leu3762Val
|
|
XM_011522531.1:c.11266C>G
(PKD1)
|
XP_011520833.1:p.Leu3756Val
|
|
XM_011522532.1:c.11212C>G
(PKD1)
|
XP_011520834.1:p.Leu3738Val
|
|
XM_011522533.1:c.11131C>G
(PKD1)
|
XP_011520835.1:p.Leu3711Val
|
|
XM_011522534.1:c.11074C>G
(PKD1)
|
XP_011520836.1:p.Leu3692Val
|
|
XM_011522535.1:c.9160C>G
(PKD1)
|
XP_011520837.1:p.Leu3054Val
|
|
XM_011522537.1:c.8338C>G
(PKD1)
|
XP_011520839.1:p.Leu2780Val
|
|
XR_932867.1:n.11353C>G
(PKD1)
|
|
|
XR_932868.1:n.11110-301C>G
(PKD1)
|
|
|
XR_932869.1:n.11110-301C>G
(PKD1)
|
|
|
XR_932870.1:n.11213C>G
(PKD1)
|
|
|
XR_933000.1:n.90-400G>C
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-400G>C
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-400G>C
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-400G>C
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-400G>C
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8215C>G
(PKD1)
|
XP_005255427.1:p.Leu2739Val
|
|
XM_011522528.3:c.11314C>G
(PKD1)
|
XP_011520830.1:p.Leu3772Val
|
|
XM_011522529.2:c.11311C>G
(PKD1)
|
XP_011520831.1:p.Leu3771Val
|
|
XM_011522537.2:c.8338C>G
(PKD1)
|
XP_011520839.1:p.Leu2780Val
|
|
XM_024450298.1:c.11380C>G
(PKD1)
|
XP_024306066.1:p.Leu3794Val
|
|
XM_024450299.1:c.11308C>G
(PKD1)
|
XP_024306067.1:p.Leu3770Val
|
|
XM_024450300.1:c.11170C>G
(PKD1)
|
XP_024306068.1:p.Leu3724Val
|
|
XM_024450301.1:c.9256C>G
(PKD1)
|
XP_024306069.1:p.Leu3086Val
|
|
NM_000296.4:c.11257C>G
(PKD1)
|
NP_000287.4:p.Leu3753Val
|
|
NM_001009944.3:c.11260C>G
(PKD1)
MANE Select
|
NP_001009944.3:p.Leu3754Val
|
|