ENST00000471862.2:n.2214T>C
(COL4A3)
|
|
|
ENST00000682257.1:n.178T>C
(COL4A3)
|
|
|
ENST00000682970.1:n.254T>C
(COL4A3)
|
|
|
ENST00000683077.1:n.1895T>C
(COL4A3)
|
|
|
ENST00000684413.1:n.2523T>C
(COL4A3)
|
|
|
ENST00000684724.1:n.377T>C
(COL4A3)
|
|
|
ENST00000396578.8:c.4956T>C
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Ala1652=
|
|
ENST00000469504.2:c.749T>C
(COL4A3)
|
ENSP00000493493.1:n.749T>C
|
|
ENST00000643388.1:c.469T>C
(COL4A3)
|
ENSP00000495177.1:p.Trp157Arg
|
|
ENST00000396578.7:c.4956T>C
(COL4A3)
|
ENSP00000379823.3:p.Ala1652=
|
|
ENST00000469504.1:n.464T>C
(COL4A3)
|
|
|
NM_000091.4:c.4956T>C , LRG_230t1:c.4956T>C
(COL4A3)
|
NP_000082.2:p.Ala1652=
|
|
NR_102371.1:n.48-6158A>G
(MFF-DT)
|
|
|
XM_005246276.2:c.4783T>C
(COL4A3)
|
XP_005246333.1:p.Trp1595Arg
|
|
XM_005246277.2:c.4851T>C
(COL4A3)
|
XP_005246334.1:p.Ala1617=
|
|
XM_011510556.1:c.3717T>C
(COL4A3)
|
XP_011508858.1:p.Ala1239=
|
|
XR_241280.2:n.4916T>C
(COL4A3)
|
|
|
XM_005246277.3:c.4851T>C
(COL4A3)
|
XP_005246334.1:p.Ala1617=
|
|
XM_011510556.2:c.3717T>C
(COL4A3)
|
XP_011508858.1:p.Ala1239=
|
|
XR_241280.3:n.4916T>C
(COL4A3)
|
|
|
NM_000091.5:c.4956T>C
(COL4A3)
MANE Select
|
NP_000082.2:p.Ala1652=
|
|