ENST00000471862.2:n.2246A>C
(COL4A3)
|
|
|
ENST00000682257.1:n.210A>C
(COL4A3)
|
|
|
ENST00000682970.1:n.286A>C
(COL4A3)
|
|
|
ENST00000683077.1:n.1927A>C
(COL4A3)
|
|
|
ENST00000684413.1:n.2555A>C
(COL4A3)
|
|
|
ENST00000684724.1:n.409A>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4988A>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Gln1663Pro
|
|
ENST00000469504.2:c.781A>C
(COL4A3)
|
ENSP00000493493.1:n.781A>C
|
|
ENST00000643388.1:c.501A>C
(COL4A3)
|
ENSP00000495177.1:p.Ser167=
|
|
ENST00000396578.7:c.4988A>C
(COL4A3)
|
ENSP00000379823.3:p.Gln1663Pro
|
|
ENST00000469504.1:n.496A>C
(COL4A3)
|
|
|
NM_000091.4:c.4988A>C , LRG_230t1:c.4988A>C
(COL4A3)
|
NP_000082.2:p.Gln1663Pro
|
|
NR_102371.1:n.48-6190T>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4815A>C
(COL4A3)
|
XP_005246333.1:p.Ser1605=
|
|
XM_005246277.2:c.4883A>C
(COL4A3)
|
XP_005246334.1:p.Gln1628Pro
|
|
XM_011510556.1:c.3749A>C
(COL4A3)
|
XP_011508858.1:p.Gln1250Pro
|
|
XR_241280.2:n.4948A>C
(COL4A3)
|
|
|
XM_005246277.3:c.4883A>C
(COL4A3)
|
XP_005246334.1:p.Gln1628Pro
|
|
XM_011510556.2:c.3749A>C
(COL4A3)
|
XP_011508858.1:p.Gln1250Pro
|
|
XR_241280.3:n.4948A>C
(COL4A3)
|
|
|
NM_000091.5:c.4988A>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Gln1663Pro
|
|