ENST00000471862.2:n.2235A>G
(COL4A3)
|
|
|
ENST00000682257.1:n.199A>G
(COL4A3)
|
|
|
ENST00000682970.1:n.275A>G
(COL4A3)
|
|
|
ENST00000683077.1:n.1916A>G
(COL4A3)
|
|
|
ENST00000684413.1:n.2544A>G
(COL4A3)
|
|
|
ENST00000684724.1:n.398A>G
(COL4A3)
|
|
|
ENST00000396578.8:c.4977A>G
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Ile1659Met
|
|
ENST00000469504.2:c.770A>G
(COL4A3)
|
ENSP00000493493.1:n.770A>G
|
|
ENST00000643388.1:c.490A>G
(COL4A3)
|
ENSP00000495177.1:p.Lys164Glu
|
|
ENST00000396578.7:c.4977A>G
(COL4A3)
|
ENSP00000379823.3:p.Ile1659Met
|
|
ENST00000469504.1:n.485A>G
(COL4A3)
|
|
|
NM_000091.4:c.4977A>G , LRG_230t1:c.4977A>G
(COL4A3)
|
NP_000082.2:p.Ile1659Met
|
|
NR_102371.1:n.48-6179T>C
(MFF-DT)
|
|
|
XM_005246276.2:c.4804A>G
(COL4A3)
|
XP_005246333.1:p.Lys1602Glu
|
|
XM_005246277.2:c.4872A>G
(COL4A3)
|
XP_005246334.1:p.Ile1624Met
|
|
XM_011510556.1:c.3738A>G
(COL4A3)
|
XP_011508858.1:p.Ile1246Met
|
|
XR_241280.2:n.4937A>G
(COL4A3)
|
|
|
XM_005246277.3:c.4872A>G
(COL4A3)
|
XP_005246334.1:p.Ile1624Met
|
|
XM_011510556.2:c.3738A>G
(COL4A3)
|
XP_011508858.1:p.Ile1246Met
|
|
XR_241280.3:n.4937A>G
(COL4A3)
|
|
|
NM_000091.5:c.4977A>G
(COL4A3)
MANE Select
|
NP_000082.2:p.Ile1659Met
|
|