ENST00000227266.10:c.1075C>T
MANE Select
|
ENSP00000227266.4:p.Leu359=
|
|
ENST00000533897.2:n.5388C>T
|
|
|
ENST00000676612.1:c.*882C>T
|
ENSP00000504440.1:n.*882C>T
|
|
ENST00000677208.1:c.*581C>T
|
ENSP00000504347.1:n.*581C>T
|
|
ENST00000677661.1:c.*752C>T
|
ENSP00000503323.1:n.*752C>T
|
|
ENST00000677802.1:c.*752C>T
|
ENSP00000504115.1:n.*752C>T
|
|
ENST00000678395.1:c.*581C>T
|
ENSP00000503123.1:n.*581C>T
|
|
ENST00000678464.1:c.1042C>T
|
ENSP00000503046.1:p.Leu348=
|
|
ENST00000678506.1:c.1036C>T
|
ENSP00000503580.1:p.Leu346=
|
|
ENST00000678520.1:c.*726C>T
|
ENSP00000503361.1:n.*726C>T
|
|
ENST00000678554.1:c.889+1810C>T
|
ENSP00000504541.1:n.889+1810C>T
|
|
ENST00000678915.1:c.943C>T
|
ENSP00000504805.1:p.Leu315=
|
|
ENST00000679224.1:c.712C>T
|
ENSP00000504475.1:p.Leu238=
|
|
ENST00000227266.9:c.1075C>T
|
ENSP00000227266.4:p.Leu359=
|
|
ENST00000533897.1:n.3809C>T
|
|
|
NM_001814.4:c.1075C>T , LRG_50t1:c.1075C>T
|
NP_001805.3:p.Leu359=
|
|
NM_001814.5:c.1075C>T
|
NP_001805.3:p.Leu359=
|
|
NM_001814.6:c.1075C>T
MANE Select
|
NP_001805.4:p.Leu359=
|
|