|
NM_000091.5:c.4235G>T
(COL4A3)
MANE Select
|
NP_000082.2:p.Gly1412Val
|
|
ENST00000396578.8:c.4235G>T
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Gly1412Val
|
|
NM_000091.4:c.4235G>T , LRG_230t1:c.4235G>T
(COL4A3)
|
NP_000082.2:p.Gly1412Val
|
|
NR_102371.1:n.243+394C>A
(MFF-DT)
|
|
|
ENST00000396578.7:c.4235G>T
(COL4A3)
|
ENSP00000379823.3:p.Gly1412Val
|
|
ENST00000469504.2:c.206G>T
(COL4A3)
|
ENSP00000493493.1:p.Gly69Val
|
|
ENST00000471862.2:n.1493G>T
(COL4A3)
|
|
|
ENST00000684413.1:n.702G>T
(COL4A3)
|
|
|
XM_005246276.2:c.4235G>T
(COL4A3)
|
XP_005246333.1:p.Gly1412Val
|
|
XM_005246277.2:c.4130G>T
(COL4A3)
|
XP_005246334.1:p.Gly1377Val
|
|
XM_005246277.3:c.4130G>T
(COL4A3)
|
XP_005246334.1:p.Gly1377Val
|
|
XM_011510555.1:c.4235G>T
(COL4A3)
|
XP_011508857.1:p.Gly1412Val
|
|
XM_011510556.1:c.2996G>T
(COL4A3)
|
XP_011508858.1:p.Gly999Val
|
|
XM_011510556.2:c.2996G>T
(COL4A3)
|
XP_011508858.1:p.Gly999Val
|
|
XR_241280.2:n.4373G>T
(COL4A3)
|
|
|
XR_241280.3:n.4373G>T
(COL4A3)
|
|
