ENST00000227266.10:c.466C>G
MANE Select
|
ENSP00000227266.4:p.Leu156Val
|
|
ENST00000527018.6:c.466C>G
|
ENSP00000432556.2:p.Leu156Val
|
|
ENST00000533897.2:n.514C>G
|
|
|
ENST00000676612.1:c.*273C>G
|
ENSP00000504440.1:n.*273C>G
|
|
ENST00000677208.1:c.319-3089C>G
|
ENSP00000504347.1:n.319-3089C>G
|
|
ENST00000677661.1:c.*143C>G
|
ENSP00000503323.1:n.*143C>G
|
|
ENST00000677802.1:c.*143C>G
|
ENSP00000504115.1:n.*143C>G
|
|
ENST00000678395.1:c.423+43C>G
|
ENSP00000503123.1:n.423+43C>G
|
|
ENST00000678464.1:c.466C>G
|
ENSP00000503046.1:p.Leu156Val
|
|
ENST00000678506.1:c.446+20C>G
|
ENSP00000503580.1:n.446+20C>G
|
|
ENST00000678520.1:c.*273C>G
|
ENSP00000503361.1:n.*273C>G
|
|
ENST00000678554.1:c.466C>G
|
ENSP00000504541.1:p.Leu156Val
|
|
ENST00000678915.1:c.466C>G
|
ENSP00000504805.1:p.Leu156Val
|
|
ENST00000679224.1:c.103C>G
|
ENSP00000504475.1:p.Leu35Val
|
|
ENST00000227266.9:c.466C>G
|
ENSP00000227266.4:p.Leu156Val
|
|
ENST00000527018.5:c.336C>G
|
|
|
ENST00000533865.5:n.488C>G
|
|
|
NM_001814.4:c.466C>G , LRG_50t1:c.466C>G
|
NP_001805.3:p.Leu156Val
|
|
NM_001814.5:c.466C>G
|
NP_001805.3:p.Leu156Val
|
|
NM_001814.6:c.466C>G
MANE Select
|
NP_001805.4:p.Leu156Val
|
|