ENST00000262304.9:c.11251C>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Gln3751Ter
|
|
ENST00000262304.8:c.11251C>T
(PKD1)
|
ENSP00000262304.4:p.Gln3751Ter
|
|
ENST00000423118.5:c.11248C>T
(PKD1)
|
ENSP00000399501.1:p.Gln3750Ter
|
|
ENST00000485120.1:n.100C>T
(PKD1)
|
|
|
ENST00000487932.5:c.5813C>T
(PKD1)
|
ENSP00000457132.1:n.5813C>T
|
|
ENST00000562425.1:c.364C>T
(PKD1)
|
|
|
ENST00000567355.1:n.414C>T
(PKD1)
|
|
|
NM_000296.3:c.11248C>T
(PKD1)
|
NP_000287.3:p.Gln3750Ter
|
|
NM_001009944.2:c.11251C>T
(PKD1)
|
NP_001009944.2:p.Gln3751Ter
|
|
XM_005255370.2:c.8206C>T
(PKD1)
|
XP_005255427.1:p.Gln2736Ter
|
|
XM_011522525.1:c.11329C>T
(PKD1)
|
XP_011520827.1:p.Gln3777Ter
|
|
XM_011522526.1:c.11326C>T
(PKD1)
|
XP_011520828.1:p.Gln3776Ter
|
|
XM_011522527.1:c.11311C>T
(PKD1)
|
XP_011520829.1:p.Gln3771Ter
|
|
XM_011522528.1:c.11305C>T
(PKD1)
|
XP_011520830.1:p.Gln3769Ter
|
|
XM_011522529.1:c.11302C>T
(PKD1)
|
XP_011520831.1:p.Gln3768Ter
|
|
XM_011522530.1:c.11275C>T
(PKD1)
|
XP_011520832.1:p.Gln3759Ter
|
|
XM_011522531.1:c.11257C>T
(PKD1)
|
XP_011520833.1:p.Gln3753Ter
|
|
XM_011522532.1:c.11203C>T
(PKD1)
|
XP_011520834.1:p.Gln3735Ter
|
|
XM_011522533.1:c.11122C>T
(PKD1)
|
XP_011520835.1:p.Gln3708Ter
|
|
XM_011522534.1:c.11065C>T
(PKD1)
|
XP_011520836.1:p.Gln3689Ter
|
|
XM_011522535.1:c.9151C>T
(PKD1)
|
XP_011520837.1:p.Gln3051Ter
|
|
XM_011522537.1:c.8329C>T
(PKD1)
|
XP_011520839.1:p.Gln2777Ter
|
|
XR_932867.1:n.11344C>T
(PKD1)
|
|
|
XR_932868.1:n.11110-310C>T
(PKD1)
|
|
|
XR_932869.1:n.11110-310C>T
(PKD1)
|
|
|
XR_932870.1:n.11204C>T
(PKD1)
|
|
|
XR_933000.1:n.90-391G>A
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-391G>A
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-391G>A
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-391G>A
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-391G>A
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8206C>T
(PKD1)
|
XP_005255427.1:p.Gln2736Ter
|
|
XM_011522528.3:c.11305C>T
(PKD1)
|
XP_011520830.1:p.Gln3769Ter
|
|
XM_011522529.2:c.11302C>T
(PKD1)
|
XP_011520831.1:p.Gln3768Ter
|
|
XM_011522537.2:c.8329C>T
(PKD1)
|
XP_011520839.1:p.Gln2777Ter
|
|
XM_024450298.1:c.11371C>T
(PKD1)
|
XP_024306066.1:p.Gln3791Ter
|
|
XM_024450299.1:c.11299C>T
(PKD1)
|
XP_024306067.1:p.Gln3767Ter
|
|
XM_024450300.1:c.11161C>T
(PKD1)
|
XP_024306068.1:p.Gln3721Ter
|
|
XM_024450301.1:c.9247C>T
(PKD1)
|
XP_024306069.1:p.Gln3083Ter
|
|
NM_000296.4:c.11248C>T
(PKD1)
|
NP_000287.4:p.Gln3750Ter
|
|
NM_001009944.3:c.11251C>T
(PKD1)
MANE Select
|
NP_001009944.3:p.Gln3751Ter
|
|