|
ENST00000262304.9:c.11179A>G
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Met3727Val
|
|
|
ENST00000262304.8:c.11179A>G
(PKD1)
|
ENSP00000262304.4:p.Met3727Val
|
|
|
ENST00000423118.5:c.11176A>G
(PKD1)
|
ENSP00000399501.1:p.Met3726Val
|
|
|
ENST00000485120.1:n.28A>G
(PKD1)
|
|
|
|
ENST00000487932.5:c.5741A>G
(PKD1)
|
ENSP00000457132.1:n.5741A>G
|
|
|
ENST00000562425.1:c.292A>G
(PKD1)
|
|
|
|
ENST00000567355.1:n.342A>G
(PKD1)
|
|
|
|
NM_000296.3:c.11176A>G
(PKD1)
|
NP_000287.3:p.Met3726Val
|
|
|
NM_001009944.2:c.11179A>G
(PKD1)
|
NP_001009944.2:p.Met3727Val
|
|
|
XM_005255370.2:c.8134A>G
(PKD1)
|
XP_005255427.1:p.Met2712Val
|
|
|
XM_011522525.1:c.11257A>G
(PKD1)
|
XP_011520827.1:p.Met3753Val
|
|
|
XM_011522526.1:c.11254A>G
(PKD1)
|
XP_011520828.1:p.Met3752Val
|
|
|
XM_011522527.1:c.11239A>G
(PKD1)
|
XP_011520829.1:p.Met3747Val
|
|
|
XM_011522528.1:c.11233A>G
(PKD1)
|
XP_011520830.1:p.Met3745Val
|
|
|
XM_011522529.1:c.11230A>G
(PKD1)
|
XP_011520831.1:p.Met3744Val
|
|
|
XM_011522530.1:c.11203A>G
(PKD1)
|
XP_011520832.1:p.Met3735Val
|
|
|
XM_011522531.1:c.11185A>G
(PKD1)
|
XP_011520833.1:p.Met3729Val
|
|
|
XM_011522532.1:c.11131A>G
(PKD1)
|
XP_011520834.1:p.Met3711Val
|
|
|
XM_011522533.1:c.11050A>G
(PKD1)
|
XP_011520835.1:p.Met3684Val
|
|
|
XM_011522534.1:c.10993A>G
(PKD1)
|
XP_011520836.1:p.Met3665Val
|
|
|
XM_011522535.1:c.9079A>G
(PKD1)
|
XP_011520837.1:p.Met3027Val
|
|
|
XM_011522537.1:c.8257A>G
(PKD1)
|
XP_011520839.1:p.Met2753Val
|
|
|
XR_932867.1:n.11272A>G
(PKD1)
|
|
|
|
XR_932868.1:n.11110-382A>G
(PKD1)
|
|
|
|
XR_932869.1:n.11110-382A>G
(PKD1)
|
|
|
|
XR_932870.1:n.11132A>G
(PKD1)
|
|
|
|
XR_933000.1:n.90-319T>C
(PKD1-AS1)
|
|
|
|
XR_933001.1:n.180-319T>C
(PKD1-AS1)
|
|
|
|
XR_933002.1:n.89-319T>C
(PKD1-AS1)
|
|
|
|
XR_933003.1:n.89-319T>C
(PKD1-AS1)
|
|
|
|
NR_135175.1:n.180-319T>C
(PKD1-AS1)
|
|
|
|
XM_005255370.3:c.8134A>G
(PKD1)
|
XP_005255427.1:p.Met2712Val
|
|
|
XM_011522528.3:c.11233A>G
(PKD1)
|
XP_011520830.1:p.Met3745Val
|
|
|
XM_011522529.2:c.11230A>G
(PKD1)
|
XP_011520831.1:p.Met3744Val
|
|
|
XM_011522537.2:c.8257A>G
(PKD1)
|
XP_011520839.1:p.Met2753Val
|
|
|
XM_024450298.1:c.11299A>G
(PKD1)
|
XP_024306066.1:p.Met3767Val
|
|
|
XM_024450299.1:c.11227A>G
(PKD1)
|
XP_024306067.1:p.Met3743Val
|
|
|
XM_024450300.1:c.11089A>G
(PKD1)
|
XP_024306068.1:p.Met3697Val
|
|
|
XM_024450301.1:c.9175A>G
(PKD1)
|
XP_024306069.1:p.Met3059Val
|
|
|
NM_000296.4:c.11176A>G
(PKD1)
|
NP_000287.4:p.Met3726Val
|
|
|
NM_001009944.3:c.11179A>G
(PKD1)
MANE Select
|
NP_001009944.3:p.Met3727Val
|
|
