ENST00000471862.2:n.1805G=
(COL4A3)
|
|
|
ENST00000683077.1:n.29G=
(COL4A3)
|
|
|
ENST00000684413.1:n.1987G=
(COL4A3)
|
|
|
ENST00000396578.8:c.4547G=
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Arg1516=
|
|
ENST00000469504.2:c.434-221G=
(COL4A3)
|
ENSP00000493493.1:n.434-221G=
|
|
ENST00000643388.1:c.233G=
(COL4A3)
|
ENSP00000495177.1:p.Arg78=
|
|
ENST00000396578.7:c.4547G=
(COL4A3)
|
ENSP00000379823.3:p.Arg1516=
|
|
ENST00000469504.1:n.149-221G=
(COL4A3)
|
|
|
NM_000091.4:c.4547G= , LRG_230t1:c.4547G=
(COL4A3)
|
NP_000082.2:p.Arg1516=
|
|
NR_102371.1:n.48-3328C=
(MFF-DT)
|
|
|
XM_005246276.2:c.4547G=
(COL4A3)
|
XP_005246333.1:p.Arg1516=
|
|
XM_005246277.2:c.4442G=
(COL4A3)
|
XP_005246334.1:p.Arg1481=
|
|
XM_011510555.1:c.4547G=
(COL4A3)
|
XP_011508857.1:p.Arg1516=
|
|
XM_011510556.1:c.3308G=
(COL4A3)
|
XP_011508858.1:p.Arg1103=
|
|
XR_241280.2:n.4601-221G=
(COL4A3)
|
|
|
XM_005246277.3:c.4442G=
(COL4A3)
|
XP_005246334.1:p.Arg1481=
|
|
XM_011510556.2:c.3308G=
(COL4A3)
|
XP_011508858.1:p.Arg1103=
|
|
XR_241280.3:n.4601-221G=
(COL4A3)
|
|
|
NM_000091.5:c.4547G=
(COL4A3)
MANE Select
|
NP_000082.2:p.Arg1516=
|
|