ENST00000471862.2:n.1609C=
(COL4A3)
|
|
|
ENST00000684413.1:n.812C=
(COL4A3)
|
|
|
ENST00000396578.8:c.4351C=
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.His1451=
|
|
ENST00000469504.2:c.322C=
(COL4A3)
|
ENSP00000493493.1:p.His108=
|
|
ENST00000643388.1:c.37C=
(COL4A3)
|
ENSP00000495177.1:p.His13=
|
|
ENST00000396578.7:c.4351C=
(COL4A3)
|
ENSP00000379823.3:p.His1451=
|
|
ENST00000469504.1:n.37C=
(COL4A3)
|
|
|
NM_000091.4:c.4351C= , LRG_230t1:c.4351C=
(COL4A3)
|
NP_000082.2:p.His1451=
|
|
NR_102371.1:n.48-2153G=
(MFF-DT)
|
|
|
XM_005246276.2:c.4351C=
(COL4A3)
|
XP_005246333.1:p.His1451=
|
|
XM_005246277.2:c.4246C=
(COL4A3)
|
XP_005246334.1:p.His1416=
|
|
XM_011510555.1:c.4351C=
(COL4A3)
|
XP_011508857.1:p.His1451=
|
|
XM_011510556.1:c.3112C=
(COL4A3)
|
XP_011508858.1:p.His1038=
|
|
XR_241280.2:n.4489C=
(COL4A3)
|
|
|
XM_005246277.3:c.4246C=
(COL4A3)
|
XP_005246334.1:p.His1416=
|
|
XM_011510556.2:c.3112C=
(COL4A3)
|
XP_011508858.1:p.His1038=
|
|
XR_241280.3:n.4489C=
(COL4A3)
|
|
|
NM_000091.5:c.4351C=
(COL4A3)
MANE Select
|
NP_000082.2:p.His1451=
|
|