ENST00000262304.9:c.10583G=
(PKD1)
MANE Select
|
ENSP00000262304.4:p.Trp3528=
|
|
ENST00000262304.8:c.10583G=
(PKD1)
|
ENSP00000262304.4:p.Trp3528=
|
|
ENST00000423118.5:c.10580G=
(PKD1)
|
ENSP00000399501.1:p.Trp3527=
|
|
ENST00000472659.1:n.20G=
(PKD1)
|
|
|
ENST00000487932.5:c.5145G=
(PKD1)
|
ENSP00000457132.1:n.5145G=
|
|
NM_000296.3:c.10580G=
(PKD1)
|
NP_000287.3:p.Trp3527=
|
|
NM_001009944.2:c.10583G=
(PKD1)
|
NP_001009944.2:p.Trp3528=
|
|
XM_005255370.2:c.7538G=
(PKD1)
|
XP_005255427.1:p.Trp2513=
|
|
XM_011522525.1:c.10661G=
(PKD1)
|
XP_011520827.1:p.Trp3554=
|
|
XM_011522526.1:c.10658G=
(PKD1)
|
XP_011520828.1:p.Trp3553=
|
|
XM_011522527.1:c.10643G=
(PKD1)
|
XP_011520829.1:p.Trp3548=
|
|
XM_011522528.1:c.10637G=
(PKD1)
|
XP_011520830.1:p.Trp3546=
|
|
XM_011522529.1:c.10634G=
(PKD1)
|
XP_011520831.1:p.Trp3545=
|
|
XM_011522530.1:c.10607G=
(PKD1)
|
XP_011520832.1:p.Trp3536=
|
|
XM_011522531.1:c.10589G=
(PKD1)
|
XP_011520833.1:p.Trp3530=
|
|
XM_011522532.1:c.10535G=
(PKD1)
|
XP_011520834.1:p.Trp3512=
|
|
XM_011522533.1:c.10454G=
(PKD1)
|
XP_011520835.1:p.Trp3485=
|
|
XM_011522534.1:c.10397G=
(PKD1)
|
XP_011520836.1:p.Trp3466=
|
|
XM_011522535.1:c.8483G=
(PKD1)
|
XP_011520837.1:p.Trp2828=
|
|
XM_011522537.1:c.7661G=
(PKD1)
|
XP_011520839.1:p.Trp2554=
|
|
XR_932867.1:n.10676G=
(PKD1)
|
|
|
XR_932868.1:n.10676G=
(PKD1)
|
|
|
XR_932869.1:n.10676G=
(PKD1)
|
|
|
XR_932870.1:n.10676G=
(PKD1)
|
|
|
XR_933000.1:n.214-551C=
(PKD1-AS1)
|
|
|
XR_933001.1:n.304-594C=
(PKD1-AS1)
|
|
|
XR_933002.1:n.213-551C=
(PKD1-AS1)
|
|
|
XR_933003.1:n.213-594C=
(PKD1-AS1)
|
|
|
NR_135175.1:n.304-594C=
(PKD1-AS1)
|
|
|
XM_005255370.3:c.7538G=
(PKD1)
|
XP_005255427.1:p.Trp2513=
|
|
XM_011522528.3:c.10637G=
(PKD1)
|
XP_011520830.1:p.Trp3546=
|
|
XM_011522529.2:c.10634G=
(PKD1)
|
XP_011520831.1:p.Trp3545=
|
|
XM_011522537.2:c.7661G=
(PKD1)
|
XP_011520839.1:p.Trp2554=
|
|
XM_024450298.1:c.10703G=
(PKD1)
|
XP_024306066.1:p.Trp3568=
|
|
XM_024450299.1:c.10631G=
(PKD1)
|
XP_024306067.1:p.Trp3544=
|
|
XM_024450300.1:c.10493G=
(PKD1)
|
XP_024306068.1:p.Trp3498=
|
|
XM_024450301.1:c.8579G=
(PKD1)
|
XP_024306069.1:p.Trp2860=
|
|
NM_000296.4:c.10580G=
(PKD1)
|
NP_000287.4:p.Trp3527=
|
|
NM_001009944.3:c.10583G=
(PKD1)
MANE Select
|
NP_001009944.3:p.Trp3528=
|
|