ENST00000471862.2:n.2218G>A
(COL4A3)
|
|
|
ENST00000682257.1:n.182G>A
(COL4A3)
|
|
|
ENST00000682970.1:n.258G>A
(COL4A3)
|
|
|
ENST00000683077.1:n.1899G>A
(COL4A3)
|
|
|
ENST00000684413.1:n.2527G>A
(COL4A3)
|
|
|
ENST00000684724.1:n.381G>A
(COL4A3)
|
|
|
ENST00000396578.8:c.4960G>A
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Glu1654Lys
|
|
ENST00000469504.2:c.753G>A
(COL4A3)
|
ENSP00000493493.1:n.753G>A
|
|
ENST00000643388.1:c.473G>A
(COL4A3)
|
ENSP00000495177.1:p.Gly158Glu
|
|
ENST00000396578.7:c.4960G>A
(COL4A3)
|
ENSP00000379823.3:p.Glu1654Lys
|
|
ENST00000469504.1:n.468G>A
(COL4A3)
|
|
|
NM_000091.4:c.4960G>A , LRG_230t1:c.4960G>A
(COL4A3)
|
NP_000082.2:p.Glu1654Lys
|
|
NR_102371.1:n.48-6162C>T
(MFF-DT)
|
|
|
XM_005246276.2:c.4787G>A
(COL4A3)
|
XP_005246333.1:p.Gly1596Glu
|
|
XM_005246277.2:c.4855G>A
(COL4A3)
|
XP_005246334.1:p.Glu1619Lys
|
|
XM_011510556.1:c.3721G>A
(COL4A3)
|
XP_011508858.1:p.Glu1241Lys
|
|
XR_241280.2:n.4920G>A
(COL4A3)
|
|
|
XM_005246277.3:c.4855G>A
(COL4A3)
|
XP_005246334.1:p.Glu1619Lys
|
|
XM_011510556.2:c.3721G>A
(COL4A3)
|
XP_011508858.1:p.Glu1241Lys
|
|
XR_241280.3:n.4920G>A
(COL4A3)
|
|
|
NM_000091.5:c.4960G>A
(COL4A3)
MANE Select
|
NP_000082.2:p.Glu1654Lys
|
|