ENST00000227266.10:c.949G>C
MANE Select
|
ENSP00000227266.4:p.Val317Leu
|
|
ENST00000533897.2:n.5262G>C
|
|
|
ENST00000676612.1:c.*756G>C
|
ENSP00000504440.1:n.*756G>C
|
|
ENST00000677208.1:c.*455G>C
|
ENSP00000504347.1:n.*455G>C
|
|
ENST00000677661.1:c.*626G>C
|
ENSP00000503323.1:n.*626G>C
|
|
ENST00000677802.1:c.*626G>C
|
ENSP00000504115.1:n.*626G>C
|
|
ENST00000678395.1:c.*455G>C
|
ENSP00000503123.1:n.*455G>C
|
|
ENST00000678464.1:c.916G>C
|
ENSP00000503046.1:p.Val306Leu
|
|
ENST00000678506.1:c.910G>C
|
ENSP00000503580.1:p.Val304Leu
|
|
ENST00000678520.1:c.*600G>C
|
ENSP00000503361.1:n.*600G>C
|
|
ENST00000678554.1:c.889+1684G>C
|
ENSP00000504541.1:n.889+1684G>C
|
|
ENST00000678915.1:c.817G>C
|
ENSP00000504805.1:p.Val273Leu
|
|
ENST00000679224.1:c.586G>C
|
ENSP00000504475.1:p.Val196Leu
|
|
ENST00000227266.9:c.949G>C
|
ENSP00000227266.4:p.Val317Leu
|
|
ENST00000533897.1:n.3683G>C
|
|
|
NM_001814.4:c.949G>C , LRG_50t1:c.949G>C
|
NP_001805.3:p.Val317Leu
|
|
NM_001814.5:c.949G>C
|
NP_001805.3:p.Val317Leu
|
|
NM_001814.6:c.949G>C
MANE Select
|
NP_001805.4:p.Val317Leu
|
|