ENST00000471862.2:n.2212G>A
(COL4A3)
|
|
|
ENST00000682257.1:n.176G>A
(COL4A3)
|
|
|
ENST00000682970.1:n.252G>A
(COL4A3)
|
|
|
ENST00000683077.1:n.1893G>A
(COL4A3)
|
|
|
ENST00000684413.1:n.2521G>A
(COL4A3)
|
|
|
ENST00000684724.1:n.375G>A
(COL4A3)
|
|
|
ENST00000396578.8:c.4954G>A
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Ala1652Thr
|
|
ENST00000469504.2:c.747G>A
(COL4A3)
|
ENSP00000493493.1:n.747G>A
|
|
ENST00000643388.1:c.467G>A
(COL4A3)
|
ENSP00000495177.1:p.Ser156Asn
|
|
ENST00000396578.7:c.4954G>A
(COL4A3)
|
ENSP00000379823.3:p.Ala1652Thr
|
|
ENST00000469504.1:n.462G>A
(COL4A3)
|
|
|
NM_000091.4:c.4954G>A , LRG_230t1:c.4954G>A
(COL4A3)
|
NP_000082.2:p.Ala1652Thr
|
|
NR_102371.1:n.48-6156C>T
(MFF-DT)
|
|
|
XM_005246276.2:c.4781G>A
(COL4A3)
|
XP_005246333.1:p.Ser1594Asn
|
|
XM_005246277.2:c.4849G>A
(COL4A3)
|
XP_005246334.1:p.Ala1617Thr
|
|
XM_011510556.1:c.3715G>A
(COL4A3)
|
XP_011508858.1:p.Ala1239Thr
|
|
XR_241280.2:n.4914G>A
(COL4A3)
|
|
|
XM_005246277.3:c.4849G>A
(COL4A3)
|
XP_005246334.1:p.Ala1617Thr
|
|
XM_011510556.2:c.3715G>A
(COL4A3)
|
XP_011508858.1:p.Ala1239Thr
|
|
XR_241280.3:n.4914G>A
(COL4A3)
|
|
|
NM_000091.5:c.4954G>A
(COL4A3)
MANE Select
|
NP_000082.2:p.Ala1652Thr
|
|