ENST00000227266.10:c.996A>C
MANE Select
|
ENSP00000227266.4:p.Lys332Asn
|
|
ENST00000533897.2:n.5309A>C
|
|
|
ENST00000676612.1:c.*803A>C
|
ENSP00000504440.1:n.*803A>C
|
|
ENST00000677208.1:c.*502A>C
|
ENSP00000504347.1:n.*502A>C
|
|
ENST00000677661.1:c.*673A>C
|
ENSP00000503323.1:n.*673A>C
|
|
ENST00000677802.1:c.*673A>C
|
ENSP00000504115.1:n.*673A>C
|
|
ENST00000678395.1:c.*502A>C
|
ENSP00000503123.1:n.*502A>C
|
|
ENST00000678464.1:c.963A>C
|
ENSP00000503046.1:p.Lys321Asn
|
|
ENST00000678506.1:c.957A>C
|
ENSP00000503580.1:p.Lys319Asn
|
|
ENST00000678520.1:c.*647A>C
|
ENSP00000503361.1:n.*647A>C
|
|
ENST00000678554.1:c.889+1731A>C
|
ENSP00000504541.1:n.889+1731A>C
|
|
ENST00000678915.1:c.864A>C
|
ENSP00000504805.1:p.Lys288Asn
|
|
ENST00000679224.1:c.633A>C
|
ENSP00000504475.1:p.Lys211Asn
|
|
ENST00000227266.9:c.996A>C
|
ENSP00000227266.4:p.Lys332Asn
|
|
ENST00000533897.1:n.3730A>C
|
|
|
NM_001814.4:c.996A>C , LRG_50t1:c.996A>C
|
NP_001805.3:p.Lys332Asn
|
|
NM_001814.5:c.996A>C
|
NP_001805.3:p.Lys332Asn
|
|
NM_001814.6:c.996A>C
MANE Select
|
NP_001805.4:p.Lys332Asn
|
|