|
ENST00000262304.9:c.10618+11G>T
(PKD1)
MANE Select
|
ENSP00000262304.4:n.10618+11G>T
|
|
|
ENST00000262304.8:c.10618+11G>T
(PKD1)
|
ENSP00000262304.4:n.10618+11G>T
|
|
|
ENST00000423118.5:c.10615+11G>T
(PKD1)
|
ENSP00000399501.1:n.10615+11G>T
|
|
|
ENST00000472659.1:n.55+11G>T
(PKD1)
|
|
|
|
ENST00000487932.5:c.5180+11G>T
(PKD1)
|
ENSP00000457132.1:n.5180+11G>T
|
|
|
NM_000296.3:c.10615+11G>T
(PKD1)
|
NP_000287.3:n.10615+11G>T
|
|
|
NM_001009944.2:c.10618+11G>T
(PKD1)
|
NP_001009944.2:n.10618+11G>T
|
|
|
XM_005255370.2:c.7573+11G>T
(PKD1)
|
XP_005255427.1:n.7573+11G>T
|
|
|
XM_011522525.1:c.10696+11G>T
(PKD1)
|
XP_011520827.1:n.10696+11G>T
|
|
|
XM_011522526.1:c.10693+11G>T
(PKD1)
|
XP_011520828.1:n.10693+11G>T
|
|
|
XM_011522527.1:c.10678+11G>T
(PKD1)
|
XP_011520829.1:n.10678+11G>T
|
|
|
XM_011522528.1:c.10672+11G>T
(PKD1)
|
XP_011520830.1:n.10672+11G>T
|
|
|
XM_011522529.1:c.10669+11G>T
(PKD1)
|
XP_011520831.1:n.10669+11G>T
|
|
|
XM_011522530.1:c.10642+11G>T
(PKD1)
|
XP_011520832.1:n.10642+11G>T
|
|
|
XM_011522531.1:c.10624+11G>T
(PKD1)
|
XP_011520833.1:n.10624+11G>T
|
|
|
XM_011522532.1:c.10570+11G>T
(PKD1)
|
XP_011520834.1:n.10570+11G>T
|
|
|
XM_011522533.1:c.10489+11G>T
(PKD1)
|
XP_011520835.1:n.10489+11G>T
|
|
|
XM_011522534.1:c.10432+11G>T
(PKD1)
|
XP_011520836.1:n.10432+11G>T
|
|
|
XM_011522535.1:c.8518+11G>T
(PKD1)
|
XP_011520837.1:n.8518+11G>T
|
|
|
XM_011522537.1:c.7696+11G>T
(PKD1)
|
XP_011520839.1:n.7696+11G>T
|
|
|
XR_932867.1:n.10711+11G>T
(PKD1)
|
|
|
|
XR_932868.1:n.10711+11G>T
(PKD1)
|
|
|
|
XR_932869.1:n.10711+11G>T
(PKD1)
|
|
|
|
XR_932870.1:n.10711+11G>T
(PKD1)
|
|
|
|
XR_933000.1:n.214-597C>A
(PKD1-AS1)
|
|
|
|
XR_933001.1:n.304-640C>A
(PKD1-AS1)
|
|
|
|
XR_933002.1:n.213-597C>A
(PKD1-AS1)
|
|
|
|
XR_933003.1:n.213-640C>A
(PKD1-AS1)
|
|
|
|
NR_135175.1:n.304-640C>A
(PKD1-AS1)
|
|
|
|
XM_005255370.3:c.7573+11G>T
(PKD1)
|
XP_005255427.1:n.7573+11G>T
|
|
|
XM_011522528.3:c.10672+11G>T
(PKD1)
|
XP_011520830.1:n.10672+11G>T
|
|
|
XM_011522529.2:c.10669+11G>T
(PKD1)
|
XP_011520831.1:n.10669+11G>T
|
|
|
XM_011522537.2:c.7696+11G>T
(PKD1)
|
XP_011520839.1:n.7696+11G>T
|
|
|
XM_024450298.1:c.10738+11G>T
(PKD1)
|
XP_024306066.1:n.10738+11G>T
|
|
|
XM_024450299.1:c.10666+11G>T
(PKD1)
|
XP_024306067.1:n.10666+11G>T
|
|
|
XM_024450300.1:c.10528+11G>T
(PKD1)
|
XP_024306068.1:n.10528+11G>T
|
|
|
XM_024450301.1:c.8614+11G>T
(PKD1)
|
XP_024306069.1:n.8614+11G>T
|
|
|
NM_000296.4:c.10615+11G>T
(PKD1)
|
NP_000287.4:n.10615+11G>T
|
|
|
NM_001009944.3:c.10618+11G>T
(PKD1)
MANE Select
|
NP_001009944.3:n.10618+11G>T
|
|
