|
ENST00000262304.9:c.11182G>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Ala3728Ser
|
|
|
ENST00000262304.8:c.11182G>T
(PKD1)
|
ENSP00000262304.4:p.Ala3728Ser
|
|
|
ENST00000423118.5:c.11179G>T
(PKD1)
|
ENSP00000399501.1:p.Ala3727Ser
|
|
|
ENST00000485120.1:n.31G>T
(PKD1)
|
|
|
|
ENST00000487932.5:c.5744G>T
(PKD1)
|
ENSP00000457132.1:n.5744G>T
|
|
|
ENST00000562425.1:c.295G>T
(PKD1)
|
|
|
|
ENST00000567355.1:n.345G>T
(PKD1)
|
|
|
|
NM_000296.3:c.11179G>T
(PKD1)
|
NP_000287.3:p.Ala3727Ser
|
|
|
NM_001009944.2:c.11182G>T
(PKD1)
|
NP_001009944.2:p.Ala3728Ser
|
|
|
XM_005255370.2:c.8137G>T
(PKD1)
|
XP_005255427.1:p.Ala2713Ser
|
|
|
XM_011522525.1:c.11260G>T
(PKD1)
|
XP_011520827.1:p.Ala3754Ser
|
|
|
XM_011522526.1:c.11257G>T
(PKD1)
|
XP_011520828.1:p.Ala3753Ser
|
|
|
XM_011522527.1:c.11242G>T
(PKD1)
|
XP_011520829.1:p.Ala3748Ser
|
|
|
XM_011522528.1:c.11236G>T
(PKD1)
|
XP_011520830.1:p.Ala3746Ser
|
|
|
XM_011522529.1:c.11233G>T
(PKD1)
|
XP_011520831.1:p.Ala3745Ser
|
|
|
XM_011522530.1:c.11206G>T
(PKD1)
|
XP_011520832.1:p.Ala3736Ser
|
|
|
XM_011522531.1:c.11188G>T
(PKD1)
|
XP_011520833.1:p.Ala3730Ser
|
|
|
XM_011522532.1:c.11134G>T
(PKD1)
|
XP_011520834.1:p.Ala3712Ser
|
|
|
XM_011522533.1:c.11053G>T
(PKD1)
|
XP_011520835.1:p.Ala3685Ser
|
|
|
XM_011522534.1:c.10996G>T
(PKD1)
|
XP_011520836.1:p.Ala3666Ser
|
|
|
XM_011522535.1:c.9082G>T
(PKD1)
|
XP_011520837.1:p.Ala3028Ser
|
|
|
XM_011522537.1:c.8260G>T
(PKD1)
|
XP_011520839.1:p.Ala2754Ser
|
|
|
XR_932867.1:n.11275G>T
(PKD1)
|
|
|
|
XR_932868.1:n.11110-379G>T
(PKD1)
|
|
|
|
XR_932869.1:n.11110-379G>T
(PKD1)
|
|
|
|
XR_932870.1:n.11135G>T
(PKD1)
|
|
|
|
XR_933000.1:n.90-322C>A
(PKD1-AS1)
|
|
|
|
XR_933001.1:n.180-322C>A
(PKD1-AS1)
|
|
|
|
XR_933002.1:n.89-322C>A
(PKD1-AS1)
|
|
|
|
XR_933003.1:n.89-322C>A
(PKD1-AS1)
|
|
|
|
NR_135175.1:n.180-322C>A
(PKD1-AS1)
|
|
|
|
XM_005255370.3:c.8137G>T
(PKD1)
|
XP_005255427.1:p.Ala2713Ser
|
|
|
XM_011522528.3:c.11236G>T
(PKD1)
|
XP_011520830.1:p.Ala3746Ser
|
|
|
XM_011522529.2:c.11233G>T
(PKD1)
|
XP_011520831.1:p.Ala3745Ser
|
|
|
XM_011522537.2:c.8260G>T
(PKD1)
|
XP_011520839.1:p.Ala2754Ser
|
|
|
XM_024450298.1:c.11302G>T
(PKD1)
|
XP_024306066.1:p.Ala3768Ser
|
|
|
XM_024450299.1:c.11230G>T
(PKD1)
|
XP_024306067.1:p.Ala3744Ser
|
|
|
XM_024450300.1:c.11092G>T
(PKD1)
|
XP_024306068.1:p.Ala3698Ser
|
|
|
XM_024450301.1:c.9178G>T
(PKD1)
|
XP_024306069.1:p.Ala3060Ser
|
|
|
NM_000296.4:c.11179G>T
(PKD1)
|
NP_000287.4:p.Ala3727Ser
|
|
|
NM_001009944.3:c.11182G>T
(PKD1)
MANE Select
|
NP_001009944.3:p.Ala3728Ser
|
|
