|
NM_000091.5:c.4207G>T
(COL4A3)
MANE Select
|
NP_000082.2:p.Gly1403Ter
|
|
ENST00000396578.8:c.4207G>T
(COL4A3)
MANE Select
|
ENSP00000379823.3:p.Gly1403Ter
|
|
NM_000091.4:c.4207G>T , LRG_230t1:c.4207G>T
(COL4A3)
|
NP_000082.2:p.Gly1403Ter
|
|
NR_102371.1:n.243+422C>A
(MFF-DT)
|
|
|
ENST00000396578.7:c.4207G>T
(COL4A3)
|
ENSP00000379823.3:p.Gly1403Ter
|
|
ENST00000469504.2:c.178G>T
(COL4A3)
|
ENSP00000493493.1:p.Gly60Ter
|
|
ENST00000471862.2:n.1465G>T
(COL4A3)
|
|
|
ENST00000684413.1:n.674G>T
(COL4A3)
|
|
|
XM_005246276.2:c.4207G>T
(COL4A3)
|
XP_005246333.1:p.Gly1403Ter
|
|
XM_005246277.2:c.4102G>T
(COL4A3)
|
XP_005246334.1:p.Gly1368Ter
|
|
XM_005246277.3:c.4102G>T
(COL4A3)
|
XP_005246334.1:p.Gly1368Ter
|
|
XM_011510555.1:c.4207G>T
(COL4A3)
|
XP_011508857.1:p.Gly1403Ter
|
|
XM_011510556.1:c.2968G>T
(COL4A3)
|
XP_011508858.1:p.Gly990Ter
|
|
XM_011510556.2:c.2968G>T
(COL4A3)
|
XP_011508858.1:p.Gly990Ter
|
|
XR_241280.2:n.4345G>T
(COL4A3)
|
|
|
XR_241280.3:n.4345G>T
(COL4A3)
|
|
