ENST00000471862.2:n.2226A>C
(COL4A3)
|
|
|
ENST00000682257.1:n.190A>C
(COL4A3)
|
|
|
ENST00000682970.1:n.266A>C
(COL4A3)
|
|
|
ENST00000683077.1:n.1907A>C
(COL4A3)
|
|
|
ENST00000684413.1:n.2535A>C
(COL4A3)
|
|
|
ENST00000684724.1:n.389A>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4968A>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Glu1656Asp
|
|
ENST00000469504.2:c.761A>C
(COL4A3)
|
ENSP00000493493.1:n.761A>C
|
|
ENST00000643388.1:c.481A>C
(COL4A3)
|
ENSP00000495177.1:p.Lys161Gln
|
|
ENST00000396578.7:c.4968A>C
(COL4A3)
|
ENSP00000379823.3:p.Glu1656Asp
|
|
ENST00000469504.1:n.476A>C
(COL4A3)
|
|
|
NM_000091.4:c.4968A>C , LRG_230t1:c.4968A>C
(COL4A3)
|
NP_000082.2:p.Glu1656Asp
|
|
NR_102371.1:n.48-6170T>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4795A>C
(COL4A3)
|
XP_005246333.1:p.Lys1599Gln
|
|
XM_005246277.2:c.4863A>C
(COL4A3)
|
XP_005246334.1:p.Glu1621Asp
|
|
XM_011510556.1:c.3729A>C
(COL4A3)
|
XP_011508858.1:p.Glu1243Asp
|
|
XR_241280.2:n.4928A>C
(COL4A3)
|
|
|
XM_005246277.3:c.4863A>C
(COL4A3)
|
XP_005246334.1:p.Glu1621Asp
|
|
XM_011510556.2:c.3729A>C
(COL4A3)
|
XP_011508858.1:p.Glu1243Asp
|
|
XR_241280.3:n.4928A>C
(COL4A3)
|
|
|
NM_000091.5:c.4968A>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Glu1656Asp
|
|