ENST00000295754.10:c.698A>C
MANE Select
|
ENSP00000295754.5:p.Asn233Thr
|
|
ENST00000672866.1:n.2294A>C
|
|
|
ENST00000295754.9:c.698A>C
|
ENSP00000295754.5:p.Asn233Thr
|
|
ENST00000359013.4:c.773A>C
|
ENSP00000351905.4:p.Asn258Thr
|
|
NM_001024847.2:c.773A>C , LRG_779t1:c.773A>C
|
NP_001020018.1:p.Asn258Thr
|
|
NM_003242.5:c.698A>C
|
NP_003233.4:p.Asn233Thr
|
|
XM_011534043.1:c.725A>C
|
XP_011532345.1:p.Asn242Thr
|
|
XM_011534044.1:c.650A>C
|
XP_011532346.1:p.Asn217Thr
|
|
XM_011534045.1:c.593A>C
|
XP_011532347.1:p.Asn198Thr
|
|
XM_011534043.2:c.725A>C
|
XP_011532345.1:p.Asn242Thr
|
|
XM_011534045.3:c.593A>C
|
XP_011532347.1:p.Asn198Thr
|
|
XM_017007106.1:c.593A>C
|
XP_016862595.1:p.Asn198Thr
|
|
NM_003242.6:c.698A>C
MANE Select
|
NP_003233.4:p.Asn233Thr
|
|