ENST00000227266.10:c.994A>T
MANE Select
|
ENSP00000227266.4:p.Lys332Ter
|
|
ENST00000533897.2:n.5307A>T
|
|
|
ENST00000676612.1:c.*801A>T
|
ENSP00000504440.1:n.*801A>T
|
|
ENST00000677208.1:c.*500A>T
|
ENSP00000504347.1:n.*500A>T
|
|
ENST00000677661.1:c.*671A>T
|
ENSP00000503323.1:n.*671A>T
|
|
ENST00000677802.1:c.*671A>T
|
ENSP00000504115.1:n.*671A>T
|
|
ENST00000678395.1:c.*500A>T
|
ENSP00000503123.1:n.*500A>T
|
|
ENST00000678464.1:c.961A>T
|
ENSP00000503046.1:p.Lys321Ter
|
|
ENST00000678506.1:c.955A>T
|
ENSP00000503580.1:p.Lys319Ter
|
|
ENST00000678520.1:c.*645A>T
|
ENSP00000503361.1:n.*645A>T
|
|
ENST00000678554.1:c.889+1729A>T
|
ENSP00000504541.1:n.889+1729A>T
|
|
ENST00000678915.1:c.862A>T
|
ENSP00000504805.1:p.Lys288Ter
|
|
ENST00000679224.1:c.631A>T
|
ENSP00000504475.1:p.Lys211Ter
|
|
ENST00000227266.9:c.994A>T
|
ENSP00000227266.4:p.Lys332Ter
|
|
ENST00000533897.1:n.3728A>T
|
|
|
NM_001814.4:c.994A>T , LRG_50t1:c.994A>T
|
NP_001805.3:p.Lys332Ter
|
|
NM_001814.5:c.994A>T
|
NP_001805.3:p.Lys332Ter
|
|
NM_001814.6:c.994A>T
MANE Select
|
NP_001805.4:p.Lys332Ter
|
|