ENST00000355480.10:c.4237G>A
(COL18A1)
|
ENSP00000347665.5:p.Glu1413Lys
|
|
ENST00000651438.1:c.3697G>A
(COL18A1)
MANE Select
|
ENSP00000498485.1:p.Glu1233Lys
|
|
ENST00000342220.9:c.1741G>A
(COL18A1)
|
ENSP00000339118.5:p.Glu581Lys
|
|
ENST00000355480.9:c.4237G>A
(COL18A1)
|
ENSP00000347665.5:p.Glu1413Lys
|
|
ENST00000359759.8:c.4942G>A
(COL18A1)
|
ENSP00000352798.4:p.Glu1648Lys
|
|
ENST00000400337.6:c.3697G>A
(COL18A1)
|
ENSP00000383191.2:p.Glu1233Lys
|
|
ENST00000417954.5:c.498-12502C>T
(SLC19A1)
|
|
|
ENST00000423214.1:c.651G>A
(COL18A1)
|
|
|
ENST00000473212.1:n.2023G>A
(COL18A1)
|
|
|
ENST00000567670.5:c.1294-12502C>T
(SLC19A1)
|
ENSP00000457278.1:n.1294-12502C>T
|
|
NM_030582.3:c.4228G>A
(COL18A1)
|
NP_085059.2:p.Glu1410Lys
|
|
NM_130444.2:c.4933G>A
(COL18A1)
|
NP_569711.2:p.Glu1645Lys
|
|
NM_130445.3:c.3688G>A
(COL18A1)
|
NP_569712.2:p.Glu1230Lys
|
|
XM_011529707.1:c.1585-8145C>T
(SLC19A1)
|
XP_011528009.1:n.1585-8145C>T
|
|
XM_017028445.2:c.1585-8145C>T
(SLC19A1)
|
XP_016883934.1:n.1585-8145C>T
|
|
NM_030582.4:c.4228G>A
(COL18A1)
|
NP_085059.2:p.Glu1410Lys
|
|
NM_130444.3:c.4933G>A
(COL18A1)
|
NP_569711.2:p.Glu1645Lys
|
|
NM_130445.4:c.3688G>A
(COL18A1)
|
NP_569712.2:p.Glu1230Lys
|
|
NM_001379500.1:c.3697G>A
(COL18A1)
MANE Select
|
NP_001366429.1:p.Glu1233Lys
|
|