ENST00000227266.10:c.999G=
MANE Select
|
ENSP00000227266.4:p.Met333=
|
|
ENST00000533897.2:n.5312G=
|
|
|
ENST00000676612.1:c.*806G=
|
ENSP00000504440.1:n.*806G=
|
|
ENST00000677208.1:c.*505G=
|
ENSP00000504347.1:n.*505G=
|
|
ENST00000677661.1:c.*676G=
|
ENSP00000503323.1:n.*676G=
|
|
ENST00000677802.1:c.*676G=
|
ENSP00000504115.1:n.*676G=
|
|
ENST00000678395.1:c.*505G=
|
ENSP00000503123.1:n.*505G=
|
|
ENST00000678464.1:c.966G=
|
ENSP00000503046.1:p.Met322=
|
|
ENST00000678506.1:c.960G=
|
ENSP00000503580.1:p.Met320=
|
|
ENST00000678520.1:c.*650G=
|
ENSP00000503361.1:n.*650G=
|
|
ENST00000678554.1:c.889+1734G=
|
ENSP00000504541.1:n.889+1734G=
|
|
ENST00000678915.1:c.867G=
|
ENSP00000504805.1:p.Met289=
|
|
ENST00000679224.1:c.636G=
|
ENSP00000504475.1:p.Met212=
|
|
ENST00000227266.9:c.999G=
|
ENSP00000227266.4:p.Met333=
|
|
ENST00000533897.1:n.3733G=
|
|
|
NM_001814.4:c.999G= , LRG_50t1:c.999G=
|
NP_001805.3:p.Met333=
|
|
NM_001814.5:c.999G=
|
NP_001805.3:p.Met333=
|
|
NM_001814.6:c.999G=
MANE Select
|
NP_001805.4:p.Met333=
|
|