ENST00000355480.10:c.3468C>T
(COL18A1)
|
ENSP00000347665.5:p.Pro1156=
|
|
ENST00000651438.1:c.2928C>T
(COL18A1)
MANE Select
|
ENSP00000498485.1:p.Pro976=
|
|
ENST00000342220.9:c.969C>T
(COL18A1)
|
ENSP00000339118.5:p.Pro323=
|
|
ENST00000355480.9:c.3468C>T
(COL18A1)
|
ENSP00000347665.5:p.Pro1156=
|
|
ENST00000359759.8:c.4173C>T
(COL18A1)
|
ENSP00000352798.4:p.Pro1391=
|
|
ENST00000400337.6:c.2928C>T
(COL18A1)
|
ENSP00000383191.2:p.Pro976=
|
|
ENST00000417954.5:c.498-6581G>A
(SLC19A1)
|
|
|
ENST00000567670.5:c.1294-6581G>A
(SLC19A1)
|
ENSP00000457278.1:n.1294-6581G>A
|
|
NM_030582.3:c.3459C>T
(COL18A1)
|
NP_085059.2:p.Pro1153=
|
|
NM_130444.2:c.4164C>T
(COL18A1)
|
NP_569711.2:p.Pro1388=
|
|
NM_130445.3:c.2919C>T
(COL18A1)
|
NP_569712.2:p.Pro973=
|
|
XM_011529707.1:c.1585-2224G>A
(SLC19A1)
|
XP_011528009.1:n.1585-2224G>A
|
|
XM_017028445.2:c.1585-2224G>A
(SLC19A1)
|
XP_016883934.1:n.1585-2224G>A
|
|
NM_030582.4:c.3459C>T
(COL18A1)
|
NP_085059.2:p.Pro1153=
|
|
NM_130444.3:c.4164C>T
(COL18A1)
|
NP_569711.2:p.Pro1388=
|
|
NM_130445.4:c.2919C>T
(COL18A1)
|
NP_569712.2:p.Pro973=
|
|
NM_001379500.1:c.2928C>T
(COL18A1)
MANE Select
|
NP_001366429.1:p.Pro976=
|
|