ENST00000295754.10:c.874G>A
MANE Select
|
ENSP00000295754.5:p.Asp292Asn
|
|
ENST00000672866.1:n.2470G>A
|
|
|
ENST00000295754.9:c.874G>A
|
ENSP00000295754.5:p.Asp292Asn
|
|
ENST00000359013.4:c.949G>A
|
ENSP00000351905.4:p.Asp317Asn
|
|
NM_001024847.2:c.949G>A , LRG_779t1:c.949G>A
|
NP_001020018.1:p.Asp317Asn
|
|
NM_003242.5:c.874G>A
|
NP_003233.4:p.Asp292Asn
|
|
XM_011534043.1:c.901G>A
|
XP_011532345.1:p.Asp301Asn
|
|
XM_011534044.1:c.826G>A
|
XP_011532346.1:p.Asp276Asn
|
|
XM_011534045.1:c.769G>A
|
XP_011532347.1:p.Asp257Asn
|
|
XM_011534043.2:c.901G>A
|
XP_011532345.1:p.Asp301Asn
|
|
XM_011534045.3:c.769G>A
|
XP_011532347.1:p.Asp257Asn
|
|
XM_017007106.1:c.769G>A
|
XP_016862595.1:p.Asp257Asn
|
|
NM_003242.6:c.874G>A
MANE Select
|
NP_003233.4:p.Asp292Asn
|
|