ENST00000471862.2:n.1783G>C
(COL4A3)
|
|
|
ENST00000683077.1:n.7G>C
(COL4A3)
|
|
|
ENST00000684413.1:n.1965G>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4525G>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Asp1509His
|
|
ENST00000469504.2:c.434-243G>C
(COL4A3)
|
ENSP00000493493.1:n.434-243G>C
|
|
ENST00000643388.1:c.211G>C
(COL4A3)
|
ENSP00000495177.1:p.Asp71His
|
|
ENST00000396578.7:c.4525G>C
(COL4A3)
|
ENSP00000379823.3:p.Asp1509His
|
|
ENST00000469504.1:n.149-243G>C
(COL4A3)
|
|
|
NM_000091.4:c.4525G>C , LRG_230t1:c.4525G>C
(COL4A3)
|
NP_000082.2:p.Asp1509His
|
|
NR_102371.1:n.48-3306C>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4525G>C
(COL4A3)
|
XP_005246333.1:p.Asp1509His
|
|
XM_005246277.2:c.4420G>C
(COL4A3)
|
XP_005246334.1:p.Asp1474His
|
|
XM_011510555.1:c.4525G>C
(COL4A3)
|
XP_011508857.1:p.Asp1509His
|
|
XM_011510556.1:c.3286G>C
(COL4A3)
|
XP_011508858.1:p.Asp1096His
|
|
XR_241280.2:n.4601-243G>C
(COL4A3)
|
|
|
XM_005246277.3:c.4420G>C
(COL4A3)
|
XP_005246334.1:p.Asp1474His
|
|
XM_011510556.2:c.3286G>C
(COL4A3)
|
XP_011508858.1:p.Asp1096His
|
|
XR_241280.3:n.4601-243G>C
(COL4A3)
|
|
|
NM_000091.5:c.4525G>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Asp1509His
|
|