ENST00000471862.2:n.2247G>A
(COL4A3)
|
|
|
ENST00000682257.1:n.211G>A
(COL4A3)
|
|
|
ENST00000682970.1:n.287G>A
(COL4A3)
|
|
|
ENST00000683077.1:n.1928G>A
(COL4A3)
|
|
|
ENST00000684413.1:n.2556G>A
(COL4A3)
|
|
|
ENST00000684724.1:n.410G>A
(COL4A3)
|
|
|
ENST00000396578.8:c.4989G>A
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Gln1663=
|
|
ENST00000469504.2:c.782G>A
(COL4A3)
|
ENSP00000493493.1:n.782G>A
|
|
ENST00000643388.1:c.502G>A
(COL4A3)
|
ENSP00000495177.1:p.Gly168Ser
|
|
ENST00000396578.7:c.4989G>A
(COL4A3)
|
ENSP00000379823.3:p.Gln1663=
|
|
ENST00000469504.1:n.497G>A
(COL4A3)
|
|
|
NM_000091.4:c.4989G>A , LRG_230t1:c.4989G>A
(COL4A3)
|
NP_000082.2:p.Gln1663=
|
|
NR_102371.1:n.48-6191C>T
(MFF-DT)
|
|
|
XM_005246276.2:c.4816G>A
(COL4A3)
|
XP_005246333.1:p.Gly1606Ser
|
|
XM_005246277.2:c.4884G>A
(COL4A3)
|
XP_005246334.1:p.Gln1628=
|
|
XM_011510556.1:c.3750G>A
(COL4A3)
|
XP_011508858.1:p.Gln1250=
|
|
XR_241280.2:n.4949G>A
(COL4A3)
|
|
|
XM_005246277.3:c.4884G>A
(COL4A3)
|
XP_005246334.1:p.Gln1628=
|
|
XM_011510556.2:c.3750G>A
(COL4A3)
|
XP_011508858.1:p.Gln1250=
|
|
XR_241280.3:n.4949G>A
(COL4A3)
|
|
|
NM_000091.5:c.4989G>A
(COL4A3)
MANE Select
|
NP_000082.2:p.Gln1663=
|
|