ENST00000262304.9:c.11167C>G
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Leu3723Val
|
|
ENST00000262304.8:c.11167C>G
(PKD1)
|
ENSP00000262304.4:p.Leu3723Val
|
|
ENST00000423118.5:c.11164C>G
(PKD1)
|
ENSP00000399501.1:p.Leu3722Val
|
|
ENST00000485120.1:n.16C>G
(PKD1)
|
|
|
ENST00000487932.5:c.5729C>G
(PKD1)
|
ENSP00000457132.1:n.5729C>G
|
|
ENST00000562425.1:c.280C>G
(PKD1)
|
|
|
ENST00000567355.1:n.330C>G
(PKD1)
|
|
|
NM_000296.3:c.11164C>G
(PKD1)
|
NP_000287.3:p.Leu3722Val
|
|
NM_001009944.2:c.11167C>G
(PKD1)
|
NP_001009944.2:p.Leu3723Val
|
|
XM_005255370.2:c.8122C>G
(PKD1)
|
XP_005255427.1:p.Leu2708Val
|
|
XM_011522525.1:c.11245C>G
(PKD1)
|
XP_011520827.1:p.Leu3749Val
|
|
XM_011522526.1:c.11242C>G
(PKD1)
|
XP_011520828.1:p.Leu3748Val
|
|
XM_011522527.1:c.11227C>G
(PKD1)
|
XP_011520829.1:p.Leu3743Val
|
|
XM_011522528.1:c.11221C>G
(PKD1)
|
XP_011520830.1:p.Leu3741Val
|
|
XM_011522529.1:c.11218C>G
(PKD1)
|
XP_011520831.1:p.Leu3740Val
|
|
XM_011522530.1:c.11191C>G
(PKD1)
|
XP_011520832.1:p.Leu3731Val
|
|
XM_011522531.1:c.11173C>G
(PKD1)
|
XP_011520833.1:p.Leu3725Val
|
|
XM_011522532.1:c.11119C>G
(PKD1)
|
XP_011520834.1:p.Leu3707Val
|
|
XM_011522533.1:c.11038C>G
(PKD1)
|
XP_011520835.1:p.Leu3680Val
|
|
XM_011522534.1:c.10981C>G
(PKD1)
|
XP_011520836.1:p.Leu3661Val
|
|
XM_011522535.1:c.9067C>G
(PKD1)
|
XP_011520837.1:p.Leu3023Val
|
|
XM_011522537.1:c.8245C>G
(PKD1)
|
XP_011520839.1:p.Leu2749Val
|
|
XR_932867.1:n.11260C>G
(PKD1)
|
|
|
XR_932868.1:n.11110-394C>G
(PKD1)
|
|
|
XR_932869.1:n.11110-394C>G
(PKD1)
|
|
|
XR_932870.1:n.11120C>G
(PKD1)
|
|
|
XR_933000.1:n.90-307G>C
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-307G>C
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-307G>C
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-307G>C
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-307G>C
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8122C>G
(PKD1)
|
XP_005255427.1:p.Leu2708Val
|
|
XM_011522528.3:c.11221C>G
(PKD1)
|
XP_011520830.1:p.Leu3741Val
|
|
XM_011522529.2:c.11218C>G
(PKD1)
|
XP_011520831.1:p.Leu3740Val
|
|
XM_011522537.2:c.8245C>G
(PKD1)
|
XP_011520839.1:p.Leu2749Val
|
|
XM_024450298.1:c.11287C>G
(PKD1)
|
XP_024306066.1:p.Leu3763Val
|
|
XM_024450299.1:c.11215C>G
(PKD1)
|
XP_024306067.1:p.Leu3739Val
|
|
XM_024450300.1:c.11077C>G
(PKD1)
|
XP_024306068.1:p.Leu3693Val
|
|
XM_024450301.1:c.9163C>G
(PKD1)
|
XP_024306069.1:p.Leu3055Val
|
|
NM_000296.4:c.11164C>G
(PKD1)
|
NP_000287.4:p.Leu3722Val
|
|
NM_001009944.3:c.11167C>G
(PKD1)
MANE Select
|
NP_001009944.3:p.Leu3723Val
|
|