|
NM_000091.5:c.3737C>G
(COL4A3)
MANE Select
|
NP_000082.2:p.Ser1246Ter
|
|
ENST00000396578.8:c.3737C>G
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Ser1246Ter
|
|
NM_000091.4:c.3737C>G , LRG_230t1:c.3737C>G
(COL4A3)
|
NP_000082.2:p.Ser1246Ter
|
|
NR_102371.1:n.243+7615G>C
(MFF-DT)
|
|
|
ENST00000396578.7:c.3737C>G
(COL4A3)
|
ENSP00000379823.3:p.Ser1246Ter
|
|
ENST00000468753.5:n.400C>G
(COL4A3)
|
|
|
ENST00000471862.1:n.155C>G
(COL4A3)
|
|
|
ENST00000471862.2:n.155C>G
(COL4A3)
|
|
|
XM_005246276.2:c.3737C>G
(COL4A3)
|
XP_005246333.1:p.Ser1246Ter
|
|
XM_005246277.2:c.3632C>G
(COL4A3)
|
XP_005246334.1:p.Ser1211Ter
|
|
XM_005246277.3:c.3632C>G
(COL4A3)
|
XP_005246334.1:p.Ser1211Ter
|
|
XM_011510555.1:c.3737C>G
(COL4A3)
|
XP_011508857.1:p.Ser1246Ter
|
|
XM_011510556.1:c.2498C>G
(COL4A3)
|
XP_011508858.1:p.Ser833Ter
|
|
XM_011510556.2:c.2498C>G
(COL4A3)
|
XP_011508858.1:p.Ser833Ter
|
|
XR_241280.2:n.3875C>G
(COL4A3)
|
|
|
XR_241280.3:n.3875C>G
(COL4A3)
|
|