ENST00000227266.10:c.993C>T
MANE Select
|
ENSP00000227266.4:p.Cys331=
|
|
ENST00000533897.2:n.5306C>T
|
|
|
ENST00000676612.1:c.*800C>T
|
ENSP00000504440.1:n.*800C>T
|
|
ENST00000677208.1:c.*499C>T
|
ENSP00000504347.1:n.*499C>T
|
|
ENST00000677661.1:c.*670C>T
|
ENSP00000503323.1:n.*670C>T
|
|
ENST00000677802.1:c.*670C>T
|
ENSP00000504115.1:n.*670C>T
|
|
ENST00000678395.1:c.*499C>T
|
ENSP00000503123.1:n.*499C>T
|
|
ENST00000678464.1:c.960C>T
|
ENSP00000503046.1:p.Cys320=
|
|
ENST00000678506.1:c.954C>T
|
ENSP00000503580.1:p.Cys318=
|
|
ENST00000678520.1:c.*644C>T
|
ENSP00000503361.1:n.*644C>T
|
|
ENST00000678554.1:c.889+1728C>T
|
ENSP00000504541.1:n.889+1728C>T
|
|
ENST00000678915.1:c.861C>T
|
ENSP00000504805.1:p.Cys287=
|
|
ENST00000679224.1:c.630C>T
|
ENSP00000504475.1:p.Cys210=
|
|
ENST00000227266.9:c.993C>T
|
ENSP00000227266.4:p.Cys331=
|
|
ENST00000533897.1:n.3727C>T
|
|
|
NM_001814.4:c.993C>T , LRG_50t1:c.993C>T
|
NP_001805.3:p.Cys331=
|
|
NM_001814.5:c.993C>T
|
NP_001805.3:p.Cys331=
|
|
NM_001814.6:c.993C>T
MANE Select
|
NP_001805.4:p.Cys331=
|
|