ENST00000397195.10:c.671+1G>T
MANE Select
|
ENSP00000380378.4:n.671+1G>T
|
|
ENST00000571495.2:n.455G>T
|
|
|
ENST00000674608.1:c.725+1G>T
|
ENSP00000501976.1:n.725+1G>T
|
|
ENST00000674717.1:c.476+1G>T
|
ENSP00000501931.1:n.476+1G>T
|
|
ENST00000675202.1:c.671+1G>T
|
ENSP00000502843.1:n.671+1G>T
|
|
ENST00000675331.1:c.671+1G>T
|
ENSP00000502031.1:n.671+1G>T
|
|
ENST00000675390.1:c.671+1G>T
|
ENSP00000501969.1:n.671+1G>T
|
|
ENST00000675574.1:n.442G>T
|
|
|
ENST00000675621.1:c.671+1G>T
|
ENSP00000502117.1:n.671+1G>T
|
|
ENST00000675764.1:c.*625+1G>T
|
ENSP00000502242.1:n.*625+1G>T
|
|
ENST00000676077.1:c.374-1302G>T
|
ENSP00000502507.1:n.374-1302G>T
|
|
ENST00000676098.1:c.671+1G>T
|
ENSP00000502735.1:n.671+1G>T
|
|
ENST00000676188.1:c.671+1G>T
|
ENSP00000502577.1:n.671+1G>T
|
|
ENST00000676353.1:c.476+1G>T
|
ENSP00000502737.1:n.476+1G>T
|
|
ENST00000397193.7:n.479+1G>T
|
|
|
ENST00000397195.9:c.671+1G>T
|
ENSP00000380378.4:n.671+1G>T
|
|
ENST00000572915.6:n.639+1G>T
|
|
|
ENST00000574468.1:c.167+1G>T
|
ENSP00000460591.1:n.167+1G>T
|
|
ENST00000574816.5:n.31-3556G>T
|
|
|
NM_000430.3:c.671+1G>T
|
NP_000421.1:n.671+1G>T
|
|
XM_011523901.1:c.725+1G>T
|
XP_011522203.1:n.725+1G>T
|
|
XM_011523902.1:c.725+1G>T
|
XP_011522204.1:n.725+1G>T
|
|
XM_011523903.1:c.725+1G>T
|
XP_011522205.1:n.725+1G>T
|
|
XM_011523904.1:c.623-1302G>T
|
XP_011522206.1:n.623-1302G>T
|
|
XM_011523901.2:c.725+1G>T
|
XP_011522203.1:n.725+1G>T
|
|
XM_011523902.3:c.725+1G>T
|
XP_011522204.1:n.725+1G>T
|
|
XM_011523903.2:c.725+1G>T
|
XP_011522205.1:n.725+1G>T
|
|
XM_017024701.1:c.671+1G>T
|
XP_016880190.1:n.671+1G>T
|
|
XM_017024702.2:c.476+1G>T
|
XP_016880191.1:n.476+1G>T
|
|
NM_000430.4:c.671+1G>T
MANE Select
|
NP_000421.1:n.671+1G>T
|
|