ENST00000227266.10:c.990A>C
MANE Select
|
ENSP00000227266.4:p.Pro330=
|
|
ENST00000533897.2:n.5303A>C
|
|
|
ENST00000676612.1:c.*797A>C
|
ENSP00000504440.1:n.*797A>C
|
|
ENST00000677208.1:c.*496A>C
|
ENSP00000504347.1:n.*496A>C
|
|
ENST00000677661.1:c.*667A>C
|
ENSP00000503323.1:n.*667A>C
|
|
ENST00000677802.1:c.*667A>C
|
ENSP00000504115.1:n.*667A>C
|
|
ENST00000678395.1:c.*496A>C
|
ENSP00000503123.1:n.*496A>C
|
|
ENST00000678464.1:c.957A>C
|
ENSP00000503046.1:p.Pro319=
|
|
ENST00000678506.1:c.951A>C
|
ENSP00000503580.1:p.Pro317=
|
|
ENST00000678520.1:c.*641A>C
|
ENSP00000503361.1:n.*641A>C
|
|
ENST00000678554.1:c.889+1725A>C
|
ENSP00000504541.1:n.889+1725A>C
|
|
ENST00000678915.1:c.858A>C
|
ENSP00000504805.1:p.Pro286=
|
|
ENST00000679224.1:c.627A>C
|
ENSP00000504475.1:p.Pro209=
|
|
ENST00000227266.9:c.990A>C
|
ENSP00000227266.4:p.Pro330=
|
|
ENST00000533897.1:n.3724A>C
|
|
|
NM_001814.4:c.990A>C , LRG_50t1:c.990A>C
|
NP_001805.3:p.Pro330=
|
|
NM_001814.5:c.990A>C
|
NP_001805.3:p.Pro330=
|
|
NM_001814.6:c.990A>C
MANE Select
|
NP_001805.4:p.Pro330=
|
|