ENST00000397195.10:c.752G>T
MANE Select
|
ENSP00000380378.4:p.Ser251Ile
|
|
ENST00000571495.2:n.1837G>T
|
|
|
ENST00000674608.1:c.806G>T
|
ENSP00000501976.1:p.Ser269Ile
|
|
ENST00000674717.1:c.557G>T
|
ENSP00000501931.1:p.Ser186Ile
|
|
ENST00000675202.1:c.752G>T
|
ENSP00000502843.1:p.Ser251Ile
|
|
ENST00000675331.1:c.752G>T
|
ENSP00000502031.1:p.Ser251Ile
|
|
ENST00000675390.1:c.752G>T
|
ENSP00000501969.1:p.Ser251Ile
|
|
ENST00000675574.1:n.1824G>T
|
|
|
ENST00000675621.1:c.752G>T
|
ENSP00000502117.1:p.Ser251Ile
|
|
ENST00000675764.1:c.*706G>T
|
ENSP00000502242.1:n.*706G>T
|
|
ENST00000676077.1:c.*70G>T
|
ENSP00000502507.1:n.*70G>T
|
|
ENST00000676098.1:c.752G>T
|
ENSP00000502735.1:p.Ser251Ile
|
|
ENST00000676188.1:c.752G>T
|
ENSP00000502577.1:p.Ser251Ile
|
|
ENST00000676353.1:c.557G>T
|
ENSP00000502737.1:p.Ser186Ile
|
|
ENST00000397193.7:n.560G>T
|
|
|
ENST00000397195.9:c.752G>T
|
ENSP00000380378.4:p.Ser251Ile
|
|
ENST00000571495.1:n.476G>T
|
|
|
ENST00000572915.6:n.676+44G>T
|
|
|
ENST00000574468.1:c.248G>T
|
ENSP00000460591.1:p.Ser83Ile
|
|
ENST00000574816.5:n.31-2174G>T
|
|
|
NM_000430.3:c.752G>T
|
NP_000421.1:p.Ser251Ile
|
|
XM_011523901.1:c.806G>T
|
XP_011522203.1:p.Ser269Ile
|
|
XM_011523902.1:c.806G>T
|
XP_011522204.1:p.Ser269Ile
|
|
XM_011523903.1:c.806G>T
|
XP_011522205.1:p.Ser269Ile
|
|
XM_011523904.1:c.*70G>T
|
XP_011522206.1:n.*70G>T
|
|
XM_011523901.2:c.806G>T
|
XP_011522203.1:p.Ser269Ile
|
|
XM_011523902.3:c.806G>T
|
XP_011522204.1:p.Ser269Ile
|
|
XM_011523903.2:c.806G>T
|
XP_011522205.1:p.Ser269Ile
|
|
XM_017024701.1:c.752G>T
|
XP_016880190.1:p.Ser251Ile
|
|
XM_017024702.2:c.557G>T
|
XP_016880191.1:p.Ser186Ile
|
|
NM_000430.4:c.752G>T
MANE Select
|
NP_000421.1:p.Ser251Ile
|
|