ENST00000471862.2:n.1916G>T
(COL4A3)
|
|
|
ENST00000682257.1:n.53G>T
(COL4A3)
|
|
|
ENST00000683077.1:n.140G>T
(COL4A3)
|
|
|
ENST00000684413.1:n.2225G>T
(COL4A3)
|
|
|
ENST00000684724.1:n.79G>T
(COL4A3)
|
|
|
ENST00000396578.8:c.4658G>T
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Gly1553Val
|
|
ENST00000469504.2:c.451G>T
(COL4A3)
|
ENSP00000493493.1:p.Val151Phe
|
|
ENST00000643388.1:c.344G>T
(COL4A3)
|
ENSP00000495177.1:p.Gly115Val
|
|
ENST00000396578.7:c.4658G>T
(COL4A3)
|
ENSP00000379823.3:p.Gly1553Val
|
|
ENST00000469504.1:n.166G>T
(COL4A3)
|
|
|
NM_000091.4:c.4658G>T , LRG_230t1:c.4658G>T
(COL4A3)
|
NP_000082.2:p.Gly1553Val
|
|
NR_102371.1:n.48-3566C>A
(MFF-DT)
|
|
|
XM_005246276.2:c.4658G>T
(COL4A3)
|
XP_005246333.1:p.Gly1553Val
|
|
XM_005246277.2:c.4553G>T
(COL4A3)
|
XP_005246334.1:p.Gly1518Val
|
|
XM_011510555.1:c.4658G>T
(COL4A3)
|
XP_011508857.1:p.Gly1553Val
|
|
XM_011510556.1:c.3419G>T
(COL4A3)
|
XP_011508858.1:p.Gly1140Val
|
|
XR_241280.2:n.4618G>T
(COL4A3)
|
|
|
XM_005246277.3:c.4553G>T
(COL4A3)
|
XP_005246334.1:p.Gly1518Val
|
|
XM_011510556.2:c.3419G>T
(COL4A3)
|
XP_011508858.1:p.Gly1140Val
|
|
XR_241280.3:n.4618G>T
(COL4A3)
|
|
|
NM_000091.5:c.4658G>T
(COL4A3)
MANE Select
|
NP_000082.2:p.Gly1553Val
|
|