ENST00000685935.1:c.*543A>T
|
ENSP00000510128.1:n.*543A>T
|
|
ENST00000686680.1:c.594A>T
|
ENSP00000508892.1:p.Thr198=
|
|
ENST00000688195.1:c.537A>T
|
ENSP00000510115.1:p.Thr179=
|
|
ENST00000688270.1:c.*230A>T
|
ENSP00000509823.1:n.*230A>T
|
|
ENST00000688618.1:c.*736A>T
|
ENSP00000509271.1:n.*736A>T
|
|
ENST00000689040.1:c.*1016A>T
|
ENSP00000508573.1:n.*1016A>T
|
|
ENST00000692097.1:c.*660A>T
|
ENSP00000509668.1:n.*660A>T
|
|
ENST00000692689.1:c.561A>T
|
ENSP00000509732.1:p.Thr187=
|
|
ENST00000693457.1:c.*1134A>T
|
ENSP00000508414.1:n.*1134A>T
|
|
ENST00000693682.1:c.*553A>T
|
ENSP00000508670.1:n.*553A>T
|
|
ENST00000258173.11:c.909A>T
MANE Select
|
ENSP00000258173.5:p.Thr303=
|
|
ENST00000258173.10:c.909A>T
|
ENSP00000258173.5:p.Thr303=
|
|
ENST00000460606.1:c.159+2566A>T
|
|
|
ENST00000562410.5:c.*711A>T
|
ENSP00000454582.1:n.*711A>T
|
|
ENST00000564318.1:n.834A>T
|
|
|
ENST00000565067.5:c.765A>T
|
ENSP00000457254.1:p.Thr255=
|
|
ENST00000568377.5:c.996A>T
|
ENSP00000476267.1:p.Thr332=
|
|
ENST00000570006.5:c.*289A>T
|
ENSP00000455520.1:n.*289A>T
|
|
NM_001077416.2:c.1068A>T
|
NP_001070884.2:p.Thr356=
|
|
NM_001077418.2:c.909A>T
|
NP_001070886.1:p.Thr303=
|
|
NR_074083.1:n.1109A>T
|
|
|
NM_001077418.3:c.909A>T
MANE Select
|
NP_001070886.1:p.Thr303=
|
|
NR_074083.2:n.1075A>T
|
|
|