|
NM_000091.5:c.3591A>G
(COL4A3)
MANE Select
|
NP_000082.2:p.Pro1197=
|
|
ENST00000396578.8:c.3591A>G
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Pro1197=
|
|
NM_000091.4:c.3591A>G , LRG_230t1:c.3591A>G
(COL4A3)
|
NP_000082.2:p.Pro1197=
|
|
NR_102371.1:n.243+7761T>C
(MFF-DT)
|
|
|
ENST00000396578.7:c.3591A>G
(COL4A3)
|
ENSP00000379823.3:p.Pro1197=
|
|
ENST00000468753.5:n.254A>G
(COL4A3)
|
|
|
ENST00000471862.1:n.9A>G
(COL4A3)
|
|
|
ENST00000471862.2:n.9A>G
(COL4A3)
|
|
|
XM_005246276.2:c.3591A>G
(COL4A3)
|
XP_005246333.1:p.Pro1197=
|
|
XM_005246277.2:c.3486A>G
(COL4A3)
|
XP_005246334.1:p.Pro1162=
|
|
XM_005246277.3:c.3486A>G
(COL4A3)
|
XP_005246334.1:p.Pro1162=
|
|
XM_006712245.2:c.*61A>G
(COL4A3)
|
XP_006712308.1:n.*61A>G
|
|
XM_006712245.3:c.*61A>G
(COL4A3)
|
XP_006712308.1:n.*61A>G
|
|
XM_011510555.1:c.3591A>G
(COL4A3)
|
XP_011508857.1:p.Pro1197=
|
|
XM_011510556.1:c.2352A>G
(COL4A3)
|
XP_011508858.1:p.Pro784=
|
|
XM_011510556.2:c.2352A>G
(COL4A3)
|
XP_011508858.1:p.Pro784=
|
|
XR_001738601.1:n.4939A>G
(COL4A3)
|
|
|
XR_241280.2:n.3729A>G
(COL4A3)
|
|
|
XR_241280.3:n.3729A>G
(COL4A3)
|
|