ENST00000262304.9:c.11236C>T
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Pro3746Ser
|
|
ENST00000262304.8:c.11236C>T
(PKD1)
|
ENSP00000262304.4:p.Pro3746Ser
|
|
ENST00000423118.5:c.11233C>T
(PKD1)
|
ENSP00000399501.1:p.Pro3745Ser
|
|
ENST00000485120.1:n.85C>T
(PKD1)
|
|
|
ENST00000487932.5:c.5798C>T
(PKD1)
|
ENSP00000457132.1:n.5798C>T
|
|
ENST00000562425.1:c.349C>T
(PKD1)
|
|
|
ENST00000567355.1:n.399C>T
(PKD1)
|
|
|
NM_000296.3:c.11233C>T
(PKD1)
|
NP_000287.3:p.Pro3745Ser
|
|
NM_001009944.2:c.11236C>T
(PKD1)
|
NP_001009944.2:p.Pro3746Ser
|
|
XM_005255370.2:c.8191C>T
(PKD1)
|
XP_005255427.1:p.Pro2731Ser
|
|
XM_011522525.1:c.11314C>T
(PKD1)
|
XP_011520827.1:p.Pro3772Ser
|
|
XM_011522526.1:c.11311C>T
(PKD1)
|
XP_011520828.1:p.Pro3771Ser
|
|
XM_011522527.1:c.11296C>T
(PKD1)
|
XP_011520829.1:p.Pro3766Ser
|
|
XM_011522528.1:c.11290C>T
(PKD1)
|
XP_011520830.1:p.Pro3764Ser
|
|
XM_011522529.1:c.11287C>T
(PKD1)
|
XP_011520831.1:p.Pro3763Ser
|
|
XM_011522530.1:c.11260C>T
(PKD1)
|
XP_011520832.1:p.Pro3754Ser
|
|
XM_011522531.1:c.11242C>T
(PKD1)
|
XP_011520833.1:p.Pro3748Ser
|
|
XM_011522532.1:c.11188C>T
(PKD1)
|
XP_011520834.1:p.Pro3730Ser
|
|
XM_011522533.1:c.11107C>T
(PKD1)
|
XP_011520835.1:p.Pro3703Ser
|
|
XM_011522534.1:c.11050C>T
(PKD1)
|
XP_011520836.1:p.Pro3684Ser
|
|
XM_011522535.1:c.9136C>T
(PKD1)
|
XP_011520837.1:p.Pro3046Ser
|
|
XM_011522537.1:c.8314C>T
(PKD1)
|
XP_011520839.1:p.Pro2772Ser
|
|
XR_932867.1:n.11329C>T
(PKD1)
|
|
|
XR_932868.1:n.11110-325C>T
(PKD1)
|
|
|
XR_932869.1:n.11110-325C>T
(PKD1)
|
|
|
XR_932870.1:n.11189C>T
(PKD1)
|
|
|
XR_933000.1:n.90-376G>A
(PKD1-AS1)
|
|
|
XR_933001.1:n.180-376G>A
(PKD1-AS1)
|
|
|
XR_933002.1:n.89-376G>A
(PKD1-AS1)
|
|
|
XR_933003.1:n.89-376G>A
(PKD1-AS1)
|
|
|
NR_135175.1:n.180-376G>A
(PKD1-AS1)
|
|
|
XM_005255370.3:c.8191C>T
(PKD1)
|
XP_005255427.1:p.Pro2731Ser
|
|
XM_011522528.3:c.11290C>T
(PKD1)
|
XP_011520830.1:p.Pro3764Ser
|
|
XM_011522529.2:c.11287C>T
(PKD1)
|
XP_011520831.1:p.Pro3763Ser
|
|
XM_011522537.2:c.8314C>T
(PKD1)
|
XP_011520839.1:p.Pro2772Ser
|
|
XM_024450298.1:c.11356C>T
(PKD1)
|
XP_024306066.1:p.Pro3786Ser
|
|
XM_024450299.1:c.11284C>T
(PKD1)
|
XP_024306067.1:p.Pro3762Ser
|
|
XM_024450300.1:c.11146C>T
(PKD1)
|
XP_024306068.1:p.Pro3716Ser
|
|
XM_024450301.1:c.9232C>T
(PKD1)
|
XP_024306069.1:p.Pro3078Ser
|
|
NM_000296.4:c.11233C>T
(PKD1)
|
NP_000287.4:p.Pro3745Ser
|
|
NM_001009944.3:c.11236C>T
(PKD1)
MANE Select
|
NP_001009944.3:p.Pro3746Ser
|
|