ENST00000471862.2:n.2488G>T
(COL4A3)
|
|
|
ENST00000682257.1:n.452G>T
(COL4A3)
|
|
|
ENST00000682970.1:n.528G>T
(COL4A3)
|
|
|
ENST00000683077.1:n.2169G>T
(COL4A3)
|
|
|
ENST00000684413.1:n.2797G>T
(COL4A3)
|
|
|
ENST00000684724.1:n.651G>T
(COL4A3)
|
|
|
ENST00000396578.8:c.*217G>T
(COL4A3)
MANE Select
|
ENSP00000379823.3:n.*217G>T
|
|
ENST00000396578.7:c.*217G>T
(COL4A3)
|
ENSP00000379823.3:n.*217G>T
|
|
NM_000091.4:c.*217G>T , LRG_230t1:c.*217G>T
(COL4A3)
|
NP_000082.2:n.*217G>T
|
|
NR_102371.1:n.48-6432C>A
(MFF-DT)
|
|
|
XM_005246276.2:c.*143G>T
(COL4A3)
|
XP_005246333.1:n.*143G>T
|
|
XM_005246277.2:c.*217G>T
(COL4A3)
|
XP_005246334.1:n.*217G>T
|
|
XM_011510556.1:c.*217G>T
(COL4A3)
|
XP_011508858.1:n.*217G>T
|
|
XR_241280.2:n.5190G>T
(COL4A3)
|
|
|
XM_005246277.3:c.*217G>T
(COL4A3)
|
XP_005246334.1:n.*217G>T
|
|
XM_011510556.2:c.*217G>T
(COL4A3)
|
XP_011508858.1:n.*217G>T
|
|
XR_241280.3:n.5190G>T
(COL4A3)
|
|
|
NM_000091.5:c.*217G>T
(COL4A3)
MANE Select
|
NP_000082.2:n.*217G>T
|
|