ENST00000227266.10:c.1054T>G
MANE Select
|
ENSP00000227266.4:p.Tyr352Asp
|
|
ENST00000533897.2:n.5367T>G
|
|
|
ENST00000676612.1:c.*861T>G
|
ENSP00000504440.1:n.*861T>G
|
|
ENST00000677208.1:c.*560T>G
|
ENSP00000504347.1:n.*560T>G
|
|
ENST00000677661.1:c.*731T>G
|
ENSP00000503323.1:n.*731T>G
|
|
ENST00000677802.1:c.*731T>G
|
ENSP00000504115.1:n.*731T>G
|
|
ENST00000678395.1:c.*560T>G
|
ENSP00000503123.1:n.*560T>G
|
|
ENST00000678464.1:c.1021T>G
|
ENSP00000503046.1:p.Tyr341Asp
|
|
ENST00000678506.1:c.1015T>G
|
ENSP00000503580.1:p.Tyr339Asp
|
|
ENST00000678520.1:c.*705T>G
|
ENSP00000503361.1:n.*705T>G
|
|
ENST00000678554.1:c.889+1789T>G
|
ENSP00000504541.1:n.889+1789T>G
|
|
ENST00000678915.1:c.922T>G
|
ENSP00000504805.1:p.Tyr308Asp
|
|
ENST00000679224.1:c.691T>G
|
ENSP00000504475.1:p.Tyr231Asp
|
|
ENST00000227266.9:c.1054T>G
|
ENSP00000227266.4:p.Tyr352Asp
|
|
ENST00000533897.1:n.3788T>G
|
|
|
NM_001814.4:c.1054T>G , LRG_50t1:c.1054T>G
|
NP_001805.3:p.Tyr352Asp
|
|
NM_001814.5:c.1054T>G
|
NP_001805.3:p.Tyr352Asp
|
|
NM_001814.6:c.1054T>G
MANE Select
|
NP_001805.4:p.Tyr352Asp
|
|