ENST00000355480.10:c.3535C>A
(COL18A1)
|
ENSP00000347665.5:p.Pro1179Thr
|
|
ENST00000651438.1:c.2995C>A
(COL18A1)
MANE Select
|
ENSP00000498485.1:p.Pro999Thr
|
|
ENST00000342220.9:c.1036C>A
(COL18A1)
|
ENSP00000339118.5:p.Pro346Thr
|
|
ENST00000355480.9:c.3535C>A
(COL18A1)
|
ENSP00000347665.5:p.Pro1179Thr
|
|
ENST00000359759.8:c.4240C>A
(COL18A1)
|
ENSP00000352798.4:p.Pro1414Thr
|
|
ENST00000400337.6:c.2995C>A
(COL18A1)
|
ENSP00000383191.2:p.Pro999Thr
|
|
ENST00000417954.5:c.498-6648G>T
(SLC19A1)
|
|
|
ENST00000567670.5:c.1294-6648G>T
(SLC19A1)
|
ENSP00000457278.1:n.1294-6648G>T
|
|
NM_030582.3:c.3526C>A
(COL18A1)
|
NP_085059.2:p.Pro1176Thr
|
|
NM_130444.2:c.4231C>A
(COL18A1)
|
NP_569711.2:p.Pro1411Thr
|
|
NM_130445.3:c.2986C>A
(COL18A1)
|
NP_569712.2:p.Pro996Thr
|
|
XM_011529707.1:c.1585-2291G>T
(SLC19A1)
|
XP_011528009.1:n.1585-2291G>T
|
|
XM_017028445.2:c.1585-2291G>T
(SLC19A1)
|
XP_016883934.1:n.1585-2291G>T
|
|
NM_030582.4:c.3526C>A
(COL18A1)
|
NP_085059.2:p.Pro1176Thr
|
|
NM_130444.3:c.4231C>A
(COL18A1)
|
NP_569711.2:p.Pro1411Thr
|
|
NM_130445.4:c.2986C>A
(COL18A1)
|
NP_569712.2:p.Pro996Thr
|
|
NM_001379500.1:c.2995C>A
(COL18A1)
MANE Select
|
NP_001366429.1:p.Pro999Thr
|
|