ENST00000471862.2:n.1852A>C
(COL4A3)
|
|
|
ENST00000683077.1:n.76A>C
(COL4A3)
|
|
|
ENST00000684413.1:n.2034A>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4594A>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Asn1532His
|
|
ENST00000469504.2:c.434-174A>C
(COL4A3)
|
ENSP00000493493.1:n.434-174A>C
|
|
ENST00000643388.1:c.280A>C
(COL4A3)
|
ENSP00000495177.1:p.Asn94His
|
|
ENST00000396578.7:c.4594A>C
(COL4A3)
|
ENSP00000379823.3:p.Asn1532His
|
|
ENST00000469504.1:n.149-174A>C
(COL4A3)
|
|
|
NM_000091.4:c.4594A>C , LRG_230t1:c.4594A>C
(COL4A3)
|
NP_000082.2:p.Asn1532His
|
|
NR_102371.1:n.48-3375T>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4594A>C
(COL4A3)
|
XP_005246333.1:p.Asn1532His
|
|
XM_005246277.2:c.4489A>C
(COL4A3)
|
XP_005246334.1:p.Asn1497His
|
|
XM_011510555.1:c.4594A>C
(COL4A3)
|
XP_011508857.1:p.Asn1532His
|
|
XM_011510556.1:c.3355A>C
(COL4A3)
|
XP_011508858.1:p.Asn1119His
|
|
XR_241280.2:n.4601-174A>C
(COL4A3)
|
|
|
XM_005246277.3:c.4489A>C
(COL4A3)
|
XP_005246334.1:p.Asn1497His
|
|
XM_011510556.2:c.3355A>C
(COL4A3)
|
XP_011508858.1:p.Asn1119His
|
|
XR_241280.3:n.4601-174A>C
(COL4A3)
|
|
|
NM_000091.5:c.4594A>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Asn1532His
|
|