ENST00000227266.10:c.1068T>C
MANE Select
|
ENSP00000227266.4:p.Asn356=
|
|
ENST00000533897.2:n.5381T>C
|
|
|
ENST00000676612.1:c.*875T>C
|
ENSP00000504440.1:n.*875T>C
|
|
ENST00000677208.1:c.*574T>C
|
ENSP00000504347.1:n.*574T>C
|
|
ENST00000677661.1:c.*745T>C
|
ENSP00000503323.1:n.*745T>C
|
|
ENST00000677802.1:c.*745T>C
|
ENSP00000504115.1:n.*745T>C
|
|
ENST00000678395.1:c.*574T>C
|
ENSP00000503123.1:n.*574T>C
|
|
ENST00000678464.1:c.1035T>C
|
ENSP00000503046.1:p.Asn345=
|
|
ENST00000678506.1:c.1029T>C
|
ENSP00000503580.1:p.Asn343=
|
|
ENST00000678520.1:c.*719T>C
|
ENSP00000503361.1:n.*719T>C
|
|
ENST00000678554.1:c.889+1803T>C
|
ENSP00000504541.1:n.889+1803T>C
|
|
ENST00000678915.1:c.936T>C
|
ENSP00000504805.1:p.Asn312=
|
|
ENST00000679224.1:c.705T>C
|
ENSP00000504475.1:p.Asn235=
|
|
ENST00000227266.9:c.1068T>C
|
ENSP00000227266.4:p.Asn356=
|
|
ENST00000533897.1:n.3802T>C
|
|
|
NM_001814.4:c.1068T>C , LRG_50t1:c.1068T>C
|
NP_001805.3:p.Asn356=
|
|
NM_001814.5:c.1068T>C
|
NP_001805.3:p.Asn356=
|
|
NM_001814.6:c.1068T>C
MANE Select
|
NP_001805.4:p.Asn356=
|
|