ENST00000227266.10:c.984T>C
MANE Select
|
ENSP00000227266.4:p.Asp328=
|
|
ENST00000533897.2:n.5297T>C
|
|
|
ENST00000676612.1:c.*791T>C
|
ENSP00000504440.1:n.*791T>C
|
|
ENST00000677208.1:c.*490T>C
|
ENSP00000504347.1:n.*490T>C
|
|
ENST00000677661.1:c.*661T>C
|
ENSP00000503323.1:n.*661T>C
|
|
ENST00000677802.1:c.*661T>C
|
ENSP00000504115.1:n.*661T>C
|
|
ENST00000678395.1:c.*490T>C
|
ENSP00000503123.1:n.*490T>C
|
|
ENST00000678464.1:c.951T>C
|
ENSP00000503046.1:p.Asp317=
|
|
ENST00000678506.1:c.945T>C
|
ENSP00000503580.1:p.Asp315=
|
|
ENST00000678520.1:c.*635T>C
|
ENSP00000503361.1:n.*635T>C
|
|
ENST00000678554.1:c.889+1719T>C
|
ENSP00000504541.1:n.889+1719T>C
|
|
ENST00000678915.1:c.852T>C
|
ENSP00000504805.1:p.Asp284=
|
|
ENST00000679224.1:c.621T>C
|
ENSP00000504475.1:p.Asp207=
|
|
ENST00000227266.9:c.984T>C
|
ENSP00000227266.4:p.Asp328=
|
|
ENST00000533897.1:n.3718T>C
|
|
|
NM_001814.4:c.984T>C , LRG_50t1:c.984T>C
|
NP_001805.3:p.Asp328=
|
|
NM_001814.5:c.984T>C
|
NP_001805.3:p.Asp328=
|
|
NM_001814.6:c.984T>C
MANE Select
|
NP_001805.4:p.Asp328=
|
|