ENST00000471862.2:n.2224G>C
(COL4A3)
|
|
|
ENST00000682257.1:n.188G>C
(COL4A3)
|
|
|
ENST00000682970.1:n.264G>C
(COL4A3)
|
|
|
ENST00000683077.1:n.1905G>C
(COL4A3)
|
|
|
ENST00000684413.1:n.2533G>C
(COL4A3)
|
|
|
ENST00000684724.1:n.387G>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4966G>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Glu1656Gln
|
|
ENST00000469504.2:c.759G>C
(COL4A3)
|
ENSP00000493493.1:n.759G>C
|
|
ENST00000643388.1:c.479G>C
(COL4A3)
|
ENSP00000495177.1:p.Arg160Thr
|
|
ENST00000396578.7:c.4966G>C
(COL4A3)
|
ENSP00000379823.3:p.Glu1656Gln
|
|
ENST00000469504.1:n.474G>C
(COL4A3)
|
|
|
NM_000091.4:c.4966G>C , LRG_230t1:c.4966G>C
(COL4A3)
|
NP_000082.2:p.Glu1656Gln
|
|
NR_102371.1:n.48-6168C>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4793G>C
(COL4A3)
|
XP_005246333.1:p.Arg1598Thr
|
|
XM_005246277.2:c.4861G>C
(COL4A3)
|
XP_005246334.1:p.Glu1621Gln
|
|
XM_011510556.1:c.3727G>C
(COL4A3)
|
XP_011508858.1:p.Glu1243Gln
|
|
XR_241280.2:n.4926G>C
(COL4A3)
|
|
|
XM_005246277.3:c.4861G>C
(COL4A3)
|
XP_005246334.1:p.Glu1621Gln
|
|
XM_011510556.2:c.3727G>C
(COL4A3)
|
XP_011508858.1:p.Glu1243Gln
|
|
XR_241280.3:n.4926G>C
(COL4A3)
|
|
|
NM_000091.5:c.4966G>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Glu1656Gln
|
|