ENST00000262304.9:c.11163G>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Glu3721Asp
|
|
ENST00000262304.8:c.11163G>T
(PKD1)
|
ENSP00000262304.4:p.Glu3721Asp
|
|
ENST00000423118.5:c.11160G>T
(PKD1)
|
ENSP00000399501.1:p.Glu3720Asp
|
|
ENST00000485120.1:n.12G>T
(PKD1)
|
|
|
ENST00000487932.5:c.5725G>T
(PKD1)
|
ENSP00000457132.1:n.5725G>T
|
|
ENST00000562425.1:c.276G>T
(PKD1)
|
|
|
ENST00000567355.1:n.326G>T
(PKD1)
|
|
|
NM_000296.3:c.11160G>T
(PKD1)
|
NP_000287.3:p.Glu3720Asp
|
|
NM_001009944.2:c.11163G>T
(PKD1)
|
NP_001009944.2:p.Glu3721Asp
|
|
XM_005255370.2:c.8118G>T
(PKD1)
|
XP_005255427.1:p.Glu2706Asp
|
|
XM_011522525.1:c.11241G>T
(PKD1)
|
XP_011520827.1:p.Glu3747Asp
|
|
XM_011522526.1:c.11238G>T
(PKD1)
|
XP_011520828.1:p.Glu3746Asp
|
|
XM_011522527.1:c.11223G>T
(PKD1)
|
XP_011520829.1:p.Glu3741Asp
|
|
XM_011522528.1:c.11217G>T
(PKD1)
|
XP_011520830.1:p.Glu3739Asp
|
|
XM_011522529.1:c.11214G>T
(PKD1)
|
XP_011520831.1:p.Glu3738Asp
|
|
XM_011522530.1:c.11187G>T
(PKD1)
|
XP_011520832.1:p.Glu3729Asp
|
|
XM_011522531.1:c.11169G>T
(PKD1)
|
XP_011520833.1:p.Glu3723Asp
|
|
XM_011522532.1:c.11115G>T
(PKD1)
|
XP_011520834.1:p.Glu3705Asp
|
|
XM_011522533.1:c.11034G>T
(PKD1)
|
XP_011520835.1:p.Glu3678Asp
|
|
XM_011522534.1:c.10977G>T
(PKD1)
|
XP_011520836.1:p.Glu3659Asp
|
|
XM_011522535.1:c.9063G>T
(PKD1)
|
XP_011520837.1:p.Glu3021Asp
|
|
XM_011522537.1:c.8241G>T
(PKD1)
|
XP_011520839.1:p.Glu2747Asp
|
|
XR_932867.1:n.11256G>T
(PKD1)
|
|
|
XR_932868.1:n.11110-398G>T
(PKD1)
|
|
|
XR_932869.1:n.11110-398G>T
(PKD1)
|
|
|
XR_932870.1:n.11116G>T
(PKD1)
|
|
|
XR_933000.1:n.90-303C>A
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-303C>A
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-303C>A
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-303C>A
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-303C>A
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8118G>T
(PKD1)
|
XP_005255427.1:p.Glu2706Asp
|
|
XM_011522528.3:c.11217G>T
(PKD1)
|
XP_011520830.1:p.Glu3739Asp
|
|
XM_011522529.2:c.11214G>T
(PKD1)
|
XP_011520831.1:p.Glu3738Asp
|
|
XM_011522537.2:c.8241G>T
(PKD1)
|
XP_011520839.1:p.Glu2747Asp
|
|
XM_024450298.1:c.11283G>T
(PKD1)
|
XP_024306066.1:p.Glu3761Asp
|
|
XM_024450299.1:c.11211G>T
(PKD1)
|
XP_024306067.1:p.Glu3737Asp
|
|
XM_024450300.1:c.11073G>T
(PKD1)
|
XP_024306068.1:p.Glu3691Asp
|
|
XM_024450301.1:c.9159G>T
(PKD1)
|
XP_024306069.1:p.Glu3053Asp
|
|
NM_000296.4:c.11160G>T
(PKD1)
|
NP_000287.4:p.Glu3720Asp
|
|
NM_001009944.3:c.11163G>T
(PKD1)
MANE Select
|
NP_001009944.3:p.Glu3721Asp
|
|