|
ENST00000471862.2:n.2382G>T
(COL4A3)
|
|
|
|
ENST00000682257.1:n.346G>T
(COL4A3)
|
|
|
|
ENST00000682970.1:n.422G>T
(COL4A3)
|
|
|
|
ENST00000683077.1:n.2063G>T
(COL4A3)
|
|
|
|
ENST00000684413.1:n.2691G>T
(COL4A3)
|
|
|
|
ENST00000684724.1:n.545G>T
(COL4A3)
|
|
|
|
ENST00000396578.8:c.*111G>T
(COL4A3)
MANE Select
|
ENSP00000379823.3:n.*111G>T
|
|
|
ENST00000396578.7:c.*111G>T
(COL4A3)
|
ENSP00000379823.3:n.*111G>T
|
|
|
NM_000091.4:c.*111G>T , LRG_230t1:c.*111G>T
(COL4A3)
|
NP_000082.2:n.*111G>T
|
|
|
NR_102371.1:n.48-6326C>A
(MFF-DT)
|
|
|
|
XM_005246276.2:c.*37G>T
(COL4A3)
|
XP_005246333.1:n.*37G>T
|
|
|
XM_005246277.2:c.*111G>T
(COL4A3)
|
XP_005246334.1:n.*111G>T
|
|
|
XM_011510556.1:c.*111G>T
(COL4A3)
|
XP_011508858.1:n.*111G>T
|
|
|
XR_241280.2:n.5084G>T
(COL4A3)
|
|
|
|
XM_005246277.3:c.*111G>T
(COL4A3)
|
XP_005246334.1:n.*111G>T
|
|
|
XM_011510556.2:c.*111G>T
(COL4A3)
|
XP_011508858.1:n.*111G>T
|
|
|
XR_241280.3:n.5084G>T
(COL4A3)
|
|
|
|
NM_000091.5:c.*111G>T
(COL4A3)
MANE Select
|
NP_000082.2:n.*111G>T
|
|
