ENST00000471862.2:n.2239C=
(COL4A3)
|
|
|
ENST00000682257.1:n.203C=
(COL4A3)
|
|
|
ENST00000682970.1:n.279C=
(COL4A3)
|
|
|
ENST00000683077.1:n.1920C=
(COL4A3)
|
|
|
ENST00000684413.1:n.2548C=
(COL4A3)
|
|
|
ENST00000684724.1:n.402C=
(COL4A3)
|
|
|
ENST00000396578.8:c.4981C=
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Arg1661=
|
|
ENST00000469504.2:c.774C=
(COL4A3)
|
ENSP00000493493.1:n.774C=
|
|
ENST00000643388.1:c.494C=
(COL4A3)
|
ENSP00000495177.1:p.Ser165=
|
|
ENST00000396578.7:c.4981C=
(COL4A3)
|
ENSP00000379823.3:p.Arg1661=
|
|
ENST00000469504.1:n.489C=
(COL4A3)
|
|
|
NM_000091.4:c.4981C= , LRG_230t1:c.4981C=
(COL4A3)
|
NP_000082.2:p.Arg1661=
|
|
NR_102371.1:n.48-6183G=
(MFF-DT)
|
|
|
XM_005246276.2:c.4808C=
(COL4A3)
|
XP_005246333.1:p.Ser1603=
|
|
XM_005246277.2:c.4876C=
(COL4A3)
|
XP_005246334.1:p.Arg1626=
|
|
XM_011510556.1:c.3742C=
(COL4A3)
|
XP_011508858.1:p.Arg1248=
|
|
XR_241280.2:n.4941C=
(COL4A3)
|
|
|
XM_005246277.3:c.4876C=
(COL4A3)
|
XP_005246334.1:p.Arg1626=
|
|
XM_011510556.2:c.3742C=
(COL4A3)
|
XP_011508858.1:p.Arg1248=
|
|
XR_241280.3:n.4941C=
(COL4A3)
|
|
|
NM_000091.5:c.4981C=
(COL4A3)
MANE Select
|
NP_000082.2:p.Arg1661=
|
|