ENST00000471862.2:n.2220A>T
(COL4A3)
|
|
|
ENST00000682257.1:n.184A>T
(COL4A3)
|
|
|
ENST00000682970.1:n.260A>T
(COL4A3)
|
|
|
ENST00000683077.1:n.1901A>T
(COL4A3)
|
|
|
ENST00000684413.1:n.2529A>T
(COL4A3)
|
|
|
ENST00000684724.1:n.383A>T
(COL4A3)
|
|
|
ENST00000396578.8:c.4962A>T
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Glu1654Asp
|
|
ENST00000469504.2:c.755A>T
(COL4A3)
|
ENSP00000493493.1:n.755A>T
|
|
ENST00000643388.1:c.475A>T
(COL4A3)
|
ENSP00000495177.1:p.Ile159Phe
|
|
ENST00000396578.7:c.4962A>T
(COL4A3)
|
ENSP00000379823.3:p.Glu1654Asp
|
|
ENST00000469504.1:n.470A>T
(COL4A3)
|
|
|
NM_000091.4:c.4962A>T , LRG_230t1:c.4962A>T
(COL4A3)
|
NP_000082.2:p.Glu1654Asp
|
|
NR_102371.1:n.48-6164T>A
(MFF-DT)
|
|
|
XM_005246276.2:c.4789A>T
(COL4A3)
|
XP_005246333.1:p.Ile1597Phe
|
|
XM_005246277.2:c.4857A>T
(COL4A3)
|
XP_005246334.1:p.Glu1619Asp
|
|
XM_011510556.1:c.3723A>T
(COL4A3)
|
XP_011508858.1:p.Glu1241Asp
|
|
XR_241280.2:n.4922A>T
(COL4A3)
|
|
|
XM_005246277.3:c.4857A>T
(COL4A3)
|
XP_005246334.1:p.Glu1619Asp
|
|
XM_011510556.2:c.3723A>T
(COL4A3)
|
XP_011508858.1:p.Glu1241Asp
|
|
XR_241280.3:n.4922A>T
(COL4A3)
|
|
|
NM_000091.5:c.4962A>T
(COL4A3)
MANE Select
|
NP_000082.2:p.Glu1654Asp
|
|