ENST00000471862.2:n.2205T>C
(COL4A3)
|
|
|
ENST00000682257.1:n.169T>C
(COL4A3)
|
|
|
ENST00000682970.1:n.245T>C
(COL4A3)
|
|
|
ENST00000683077.1:n.1886T>C
(COL4A3)
|
|
|
ENST00000684413.1:n.2514T>C
(COL4A3)
|
|
|
ENST00000684724.1:n.368T>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4947T>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Thr1649=
|
|
ENST00000469504.2:c.740T>C
(COL4A3)
|
ENSP00000493493.1:n.740T>C
|
|
ENST00000643388.1:c.460T>C
(COL4A3)
|
ENSP00000495177.1:p.Cys154Arg
|
|
ENST00000396578.7:c.4947T>C
(COL4A3)
|
ENSP00000379823.3:p.Thr1649=
|
|
ENST00000469504.1:n.455T>C
(COL4A3)
|
|
|
NM_000091.4:c.4947T>C , LRG_230t1:c.4947T>C
(COL4A3)
|
NP_000082.2:p.Thr1649=
|
|
NR_102371.1:n.48-6149A>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4774T>C
(COL4A3)
|
XP_005246333.1:p.Cys1592Arg
|
|
XM_005246277.2:c.4842T>C
(COL4A3)
|
XP_005246334.1:p.Thr1614=
|
|
XM_011510556.1:c.3708T>C
(COL4A3)
|
XP_011508858.1:p.Thr1236=
|
|
XR_241280.2:n.4907T>C
(COL4A3)
|
|
|
XM_005246277.3:c.4842T>C
(COL4A3)
|
XP_005246334.1:p.Thr1614=
|
|
XM_011510556.2:c.3708T>C
(COL4A3)
|
XP_011508858.1:p.Thr1236=
|
|
XR_241280.3:n.4907T>C
(COL4A3)
|
|
|
NM_000091.5:c.4947T>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Thr1649=
|
|