ENST00000227266.10:c.995A>C
MANE Select
|
ENSP00000227266.4:p.Lys332Thr
|
|
ENST00000533897.2:n.5308A>C
|
|
|
ENST00000676612.1:c.*802A>C
|
ENSP00000504440.1:n.*802A>C
|
|
ENST00000677208.1:c.*501A>C
|
ENSP00000504347.1:n.*501A>C
|
|
ENST00000677661.1:c.*672A>C
|
ENSP00000503323.1:n.*672A>C
|
|
ENST00000677802.1:c.*672A>C
|
ENSP00000504115.1:n.*672A>C
|
|
ENST00000678395.1:c.*501A>C
|
ENSP00000503123.1:n.*501A>C
|
|
ENST00000678464.1:c.962A>C
|
ENSP00000503046.1:p.Lys321Thr
|
|
ENST00000678506.1:c.956A>C
|
ENSP00000503580.1:p.Lys319Thr
|
|
ENST00000678520.1:c.*646A>C
|
ENSP00000503361.1:n.*646A>C
|
|
ENST00000678554.1:c.889+1730A>C
|
ENSP00000504541.1:n.889+1730A>C
|
|
ENST00000678915.1:c.863A>C
|
ENSP00000504805.1:p.Lys288Thr
|
|
ENST00000679224.1:c.632A>C
|
ENSP00000504475.1:p.Lys211Thr
|
|
ENST00000227266.9:c.995A>C
|
ENSP00000227266.4:p.Lys332Thr
|
|
ENST00000533897.1:n.3729A>C
|
|
|
NM_001814.4:c.995A>C , LRG_50t1:c.995A>C
|
NP_001805.3:p.Lys332Thr
|
|
NM_001814.5:c.995A>C
|
NP_001805.3:p.Lys332Thr
|
|
NM_001814.6:c.995A>C
MANE Select
|
NP_001805.4:p.Lys332Thr
|
|