ENST00000471862.2:n.2250G>A
(COL4A3)
|
|
|
ENST00000682257.1:n.214G>A
(COL4A3)
|
|
|
ENST00000682970.1:n.290G>A
(COL4A3)
|
|
|
ENST00000683077.1:n.1931G>A
(COL4A3)
|
|
|
ENST00000684413.1:n.2559G>A
(COL4A3)
|
|
|
ENST00000684724.1:n.413G>A
(COL4A3)
|
|
|
ENST00000396578.8:c.4992G>A
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Val1664=
|
|
ENST00000469504.2:c.785G>A
(COL4A3)
|
ENSP00000493493.1:n.785G>A
|
|
ENST00000643388.1:c.505G>A
(COL4A3)
|
ENSP00000495177.1:p.Val169Met
|
|
ENST00000396578.7:c.4992G>A
(COL4A3)
|
ENSP00000379823.3:p.Val1664=
|
|
ENST00000469504.1:n.500G>A
(COL4A3)
|
|
|
NM_000091.4:c.4992G>A , LRG_230t1:c.4992G>A
(COL4A3)
|
NP_000082.2:p.Val1664=
|
|
NR_102371.1:n.48-6194C>T
(MFF-DT)
|
|
|
XM_005246276.2:c.4819G>A
(COL4A3)
|
XP_005246333.1:p.Val1607Met
|
|
XM_005246277.2:c.4887G>A
(COL4A3)
|
XP_005246334.1:p.Val1629=
|
|
XM_011510556.1:c.3753G>A
(COL4A3)
|
XP_011508858.1:p.Val1251=
|
|
XR_241280.2:n.4952G>A
(COL4A3)
|
|
|
XM_005246277.3:c.4887G>A
(COL4A3)
|
XP_005246334.1:p.Val1629=
|
|
XM_011510556.2:c.3753G>A
(COL4A3)
|
XP_011508858.1:p.Val1251=
|
|
XR_241280.3:n.4952G>A
(COL4A3)
|
|
|
NM_000091.5:c.4992G>A
(COL4A3)
MANE Select
|
NP_000082.2:p.Val1664=
|
|