ENST00000227266.10:c.945G>T
MANE Select
|
ENSP00000227266.4:p.Gly315=
|
|
ENST00000533897.2:n.5258G>T
|
|
|
ENST00000676612.1:c.*752G>T
|
ENSP00000504440.1:n.*752G>T
|
|
ENST00000677208.1:c.*451G>T
|
ENSP00000504347.1:n.*451G>T
|
|
ENST00000677661.1:c.*622G>T
|
ENSP00000503323.1:n.*622G>T
|
|
ENST00000677802.1:c.*622G>T
|
ENSP00000504115.1:n.*622G>T
|
|
ENST00000678395.1:c.*451G>T
|
ENSP00000503123.1:n.*451G>T
|
|
ENST00000678464.1:c.912G>T
|
ENSP00000503046.1:p.Gly304=
|
|
ENST00000678506.1:c.906G>T
|
ENSP00000503580.1:p.Gly302=
|
|
ENST00000678520.1:c.*596G>T
|
ENSP00000503361.1:n.*596G>T
|
|
ENST00000678554.1:c.889+1680G>T
|
ENSP00000504541.1:n.889+1680G>T
|
|
ENST00000678915.1:c.813G>T
|
ENSP00000504805.1:p.Gly271=
|
|
ENST00000679224.1:c.582G>T
|
ENSP00000504475.1:p.Gly194=
|
|
ENST00000227266.9:c.945G>T
|
ENSP00000227266.4:p.Gly315=
|
|
ENST00000533897.1:n.3679G>T
|
|
|
NM_001814.4:c.945G>T , LRG_50t1:c.945G>T
|
NP_001805.3:p.Gly315=
|
|
NM_001814.5:c.945G>T
|
NP_001805.3:p.Gly315=
|
|
NM_001814.6:c.945G>T
MANE Select
|
NP_001805.4:p.Gly315=
|
|