ENST00000227266.10:c.981T>C
MANE Select
|
ENSP00000227266.4:p.Thr327=
|
|
ENST00000533897.2:n.5294T>C
|
|
|
ENST00000676612.1:c.*788T>C
|
ENSP00000504440.1:n.*788T>C
|
|
ENST00000677208.1:c.*487T>C
|
ENSP00000504347.1:n.*487T>C
|
|
ENST00000677661.1:c.*658T>C
|
ENSP00000503323.1:n.*658T>C
|
|
ENST00000677802.1:c.*658T>C
|
ENSP00000504115.1:n.*658T>C
|
|
ENST00000678395.1:c.*487T>C
|
ENSP00000503123.1:n.*487T>C
|
|
ENST00000678464.1:c.948T>C
|
ENSP00000503046.1:p.Thr316=
|
|
ENST00000678506.1:c.942T>C
|
ENSP00000503580.1:p.Thr314=
|
|
ENST00000678520.1:c.*632T>C
|
ENSP00000503361.1:n.*632T>C
|
|
ENST00000678554.1:c.889+1716T>C
|
ENSP00000504541.1:n.889+1716T>C
|
|
ENST00000678915.1:c.849T>C
|
ENSP00000504805.1:p.Thr283=
|
|
ENST00000679224.1:c.618T>C
|
ENSP00000504475.1:p.Thr206=
|
|
ENST00000227266.9:c.981T>C
|
ENSP00000227266.4:p.Thr327=
|
|
ENST00000533897.1:n.3715T>C
|
|
|
NM_001814.4:c.981T>C , LRG_50t1:c.981T>C
|
NP_001805.3:p.Thr327=
|
|
NM_001814.5:c.981T>C
|
NP_001805.3:p.Thr327=
|
|
NM_001814.6:c.981T>C
MANE Select
|
NP_001805.4:p.Thr327=
|
|