ENST00000355480.10:c.3382G>T
(COL18A1)
|
ENSP00000347665.5:p.Gly1128Cys
|
|
ENST00000651438.1:c.2842G>T
(COL18A1)
MANE Select
|
ENSP00000498485.1:p.Gly948Cys
|
|
ENST00000342220.9:c.883G>T
(COL18A1)
|
ENSP00000339118.5:p.Gly295Cys
|
|
ENST00000355480.9:c.3382G>T
(COL18A1)
|
ENSP00000347665.5:p.Gly1128Cys
|
|
ENST00000359759.8:c.4087G>T
(COL18A1)
|
ENSP00000352798.4:p.Gly1363Cys
|
|
ENST00000400337.6:c.2842G>T
(COL18A1)
|
ENSP00000383191.2:p.Gly948Cys
|
|
ENST00000417954.5:c.498-5918C>A
(SLC19A1)
|
|
|
ENST00000567670.5:c.1294-5918C>A
(SLC19A1)
|
ENSP00000457278.1:n.1294-5918C>A
|
|
XM_011529707.1:c.1585-1561C>A
(SLC19A1)
|
XP_011528009.1:n.1585-1561C>A
|
|
XM_017028445.2:c.1585-1561C>A
(SLC19A1)
|
XP_016883934.1:n.1585-1561C>A
|
|
NM_001379500.1:c.2842G>T
(COL18A1)
MANE Select
|
NP_001366429.1:p.Gly948Cys
|
|