ENST00000471862.2:n.2198C>G
(COL4A3)
|
|
|
ENST00000682257.1:n.162C>G
(COL4A3)
|
|
|
ENST00000682970.1:n.238C>G
(COL4A3)
|
|
|
ENST00000683077.1:n.1879C>G
(COL4A3)
|
|
|
ENST00000684413.1:n.2507C>G
(COL4A3)
|
|
|
ENST00000684724.1:n.361C>G
(COL4A3)
|
|
|
ENST00000396578.8:c.4940C>G
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Pro1647Arg
|
|
ENST00000469504.2:c.733C>G
(COL4A3)
|
ENSP00000493493.1:n.733C>G
|
|
ENST00000643388.1:c.453C>G
(COL4A3)
|
ENSP00000495177.1:p.Ser151=
|
|
ENST00000396578.7:c.4940C>G
(COL4A3)
|
ENSP00000379823.3:p.Pro1647Arg
|
|
ENST00000469504.1:n.448C>G
(COL4A3)
|
|
|
NM_000091.4:c.4940C>G , LRG_230t1:c.4940C>G
(COL4A3)
|
NP_000082.2:p.Pro1647Arg
|
|
NR_102371.1:n.48-6142G>C
(MFF-DT)
|
|
|
XM_005246276.2:c.4767C>G
(COL4A3)
|
XP_005246333.1:p.Ser1589=
|
|
XM_005246277.2:c.4835C>G
(COL4A3)
|
XP_005246334.1:p.Pro1612Arg
|
|
XM_011510556.1:c.3701C>G
(COL4A3)
|
XP_011508858.1:p.Pro1234Arg
|
|
XR_241280.2:n.4900C>G
(COL4A3)
|
|
|
XM_005246277.3:c.4835C>G
(COL4A3)
|
XP_005246334.1:p.Pro1612Arg
|
|
XM_011510556.2:c.3701C>G
(COL4A3)
|
XP_011508858.1:p.Pro1234Arg
|
|
XR_241280.3:n.4900C>G
(COL4A3)
|
|
|
NM_000091.5:c.4940C>G
(COL4A3)
MANE Select
|
NP_000082.2:p.Pro1647Arg
|
|