ENST00000355480.10:c.4339C>G
(COL18A1)
|
ENSP00000347665.5:p.His1447Asp
|
|
ENST00000651438.1:c.3799C>G
(COL18A1)
MANE Select
|
ENSP00000498485.1:p.His1267Asp
|
|
ENST00000342220.9:c.1843C>G
(COL18A1)
|
ENSP00000339118.5:p.His615Asp
|
|
ENST00000355480.9:c.4339C>G
(COL18A1)
|
ENSP00000347665.5:p.His1447Asp
|
|
ENST00000359759.8:c.5044C>G
(COL18A1)
|
ENSP00000352798.4:p.His1682Asp
|
|
ENST00000400337.6:c.3799C>G
(COL18A1)
|
ENSP00000383191.2:p.His1267Asp
|
|
ENST00000417954.5:c.498-12604G>C
(SLC19A1)
|
|
|
ENST00000423214.1:c.753C>G
(COL18A1)
|
|
|
ENST00000473212.1:n.2125C>G
(COL18A1)
|
|
|
ENST00000567670.5:c.1294-12604G>C
(SLC19A1)
|
ENSP00000457278.1:n.1294-12604G>C
|
|
NM_030582.3:c.4330C>G
(COL18A1)
|
NP_085059.2:p.His1444Asp
|
|
NM_130444.2:c.5035C>G
(COL18A1)
|
NP_569711.2:p.His1679Asp
|
|
NM_130445.3:c.3790C>G
(COL18A1)
|
NP_569712.2:p.His1264Asp
|
|
XM_011529707.1:c.1585-8247G>C
(SLC19A1)
|
XP_011528009.1:n.1585-8247G>C
|
|
XM_017028445.2:c.1585-8247G>C
(SLC19A1)
|
XP_016883934.1:n.1585-8247G>C
|
|
NM_030582.4:c.4330C>G
(COL18A1)
|
NP_085059.2:p.His1444Asp
|
|
NM_130444.3:c.5035C>G
(COL18A1)
|
NP_569711.2:p.His1679Asp
|
|
NM_130445.4:c.3790C>G
(COL18A1)
|
NP_569712.2:p.His1264Asp
|
|
NM_001379500.1:c.3799C>G
(COL18A1)
MANE Select
|
NP_001366429.1:p.His1267Asp
|
|