ENST00000471862.2:n.2192C>G
(COL4A3)
|
|
|
ENST00000682257.1:n.156C>G
(COL4A3)
|
|
|
ENST00000682970.1:n.232C>G
(COL4A3)
|
|
|
ENST00000683077.1:n.1873C>G
(COL4A3)
|
|
|
ENST00000684413.1:n.2501C>G
(COL4A3)
|
|
|
ENST00000684724.1:n.355C>G
(COL4A3)
|
|
|
ENST00000396578.8:c.4934C>G
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Pro1645Arg
|
|
ENST00000469504.2:c.727C>G
(COL4A3)
|
ENSP00000493493.1:n.727C>G
|
|
ENST00000643388.1:c.447C>G
(COL4A3)
|
ENSP00000495177.1:p.Ala149=
|
|
ENST00000396578.7:c.4934C>G
(COL4A3)
|
ENSP00000379823.3:p.Pro1645Arg
|
|
ENST00000469504.1:n.442C>G
(COL4A3)
|
|
|
NM_000091.4:c.4934C>G , LRG_230t1:c.4934C>G
(COL4A3)
|
NP_000082.2:p.Pro1645Arg
|
|
NR_102371.1:n.48-6136G>C
(MFF-DT)
|
|
|
XM_005246276.2:c.4761C>G
(COL4A3)
|
XP_005246333.1:p.Ala1587=
|
|
XM_005246277.2:c.4829C>G
(COL4A3)
|
XP_005246334.1:p.Pro1610Arg
|
|
XM_011510556.1:c.3695C>G
(COL4A3)
|
XP_011508858.1:p.Pro1232Arg
|
|
XR_241280.2:n.4894C>G
(COL4A3)
|
|
|
XM_005246277.3:c.4829C>G
(COL4A3)
|
XP_005246334.1:p.Pro1610Arg
|
|
XM_011510556.2:c.3695C>G
(COL4A3)
|
XP_011508858.1:p.Pro1232Arg
|
|
XR_241280.3:n.4894C>G
(COL4A3)
|
|
|
NM_000091.5:c.4934C>G
(COL4A3)
MANE Select
|
NP_000082.2:p.Pro1645Arg
|
|