ENST00000355480.10:c.3440C>A
(COL18A1)
|
ENSP00000347665.5:p.Pro1147His
|
|
ENST00000651438.1:c.2900C>A
(COL18A1)
MANE Select
|
ENSP00000498485.1:p.Pro967His
|
|
ENST00000342220.9:c.941C>A
(COL18A1)
|
ENSP00000339118.5:p.Pro314His
|
|
ENST00000355480.9:c.3440C>A
(COL18A1)
|
ENSP00000347665.5:p.Pro1147His
|
|
ENST00000359759.8:c.4145C>A
(COL18A1)
|
ENSP00000352798.4:p.Pro1382His
|
|
ENST00000400337.6:c.2900C>A
(COL18A1)
|
ENSP00000383191.2:p.Pro967His
|
|
ENST00000417954.5:c.498-6553G>T
(SLC19A1)
|
|
|
ENST00000567670.5:c.1294-6553G>T
(SLC19A1)
|
ENSP00000457278.1:n.1294-6553G>T
|
|
NM_030582.3:c.3431C>A
(COL18A1)
|
NP_085059.2:p.Pro1144His
|
|
NM_130444.2:c.4136C>A
(COL18A1)
|
NP_569711.2:p.Pro1379His
|
|
NM_130445.3:c.2891C>A
(COL18A1)
|
NP_569712.2:p.Pro964His
|
|
XM_011529707.1:c.1585-2196G>T
(SLC19A1)
|
XP_011528009.1:n.1585-2196G>T
|
|
XM_017028445.2:c.1585-2196G>T
(SLC19A1)
|
XP_016883934.1:n.1585-2196G>T
|
|
NM_030582.4:c.3431C>A
(COL18A1)
|
NP_085059.2:p.Pro1144His
|
|
NM_130444.3:c.4136C>A
(COL18A1)
|
NP_569711.2:p.Pro1379His
|
|
NM_130445.4:c.2891C>A
(COL18A1)
|
NP_569712.2:p.Pro964His
|
|
NM_001379500.1:c.2900C>A
(COL18A1)
MANE Select
|
NP_001366429.1:p.Pro967His
|
|