ENST00000471862.2:n.2242T>A
(COL4A3)
|
|
|
ENST00000682257.1:n.206T>A
(COL4A3)
|
|
|
ENST00000682970.1:n.282T>A
(COL4A3)
|
|
|
ENST00000683077.1:n.1923T>A
(COL4A3)
|
|
|
ENST00000684413.1:n.2551T>A
(COL4A3)
|
|
|
ENST00000684724.1:n.405T>A
(COL4A3)
|
|
|
ENST00000396578.8:c.4984T>A
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Cys1662Ser
|
|
ENST00000469504.2:c.777T>A
(COL4A3)
|
ENSP00000493493.1:n.777T>A
|
|
ENST00000643388.1:c.497T>A
(COL4A3)
|
ENSP00000495177.1:p.Leu166Gln
|
|
ENST00000396578.7:c.4984T>A
(COL4A3)
|
ENSP00000379823.3:p.Cys1662Ser
|
|
ENST00000469504.1:n.492T>A
(COL4A3)
|
|
|
NM_000091.4:c.4984T>A , LRG_230t1:c.4984T>A
(COL4A3)
|
NP_000082.2:p.Cys1662Ser
|
|
NR_102371.1:n.48-6186A>T
(MFF-DT)
|
|
|
XM_005246276.2:c.4811T>A
(COL4A3)
|
XP_005246333.1:p.Leu1604Gln
|
|
XM_005246277.2:c.4879T>A
(COL4A3)
|
XP_005246334.1:p.Cys1627Ser
|
|
XM_011510556.1:c.3745T>A
(COL4A3)
|
XP_011508858.1:p.Cys1249Ser
|
|
XR_241280.2:n.4944T>A
(COL4A3)
|
|
|
XM_005246277.3:c.4879T>A
(COL4A3)
|
XP_005246334.1:p.Cys1627Ser
|
|
XM_011510556.2:c.3745T>A
(COL4A3)
|
XP_011508858.1:p.Cys1249Ser
|
|
XR_241280.3:n.4944T>A
(COL4A3)
|
|
|
NM_000091.5:c.4984T>A
(COL4A3)
MANE Select
|
NP_000082.2:p.Cys1662Ser
|
|