ENST00000295754.10:c.1091A>G
MANE Select
|
ENSP00000295754.5:p.Asp364Gly
|
|
ENST00000672866.1:n.2687A>G
|
|
|
ENST00000295754.9:c.1091A>G
|
ENSP00000295754.5:p.Asp364Gly
|
|
ENST00000359013.4:c.1166A>G
|
ENSP00000351905.4:p.Asp389Gly
|
|
NM_001024847.2:c.1166A>G , LRG_779t1:c.1166A>G
|
NP_001020018.1:p.Asp389Gly
|
|
NM_003242.5:c.1091A>G
|
NP_003233.4:p.Asp364Gly
|
|
XM_011534043.1:c.1118A>G
|
XP_011532345.1:p.Asp373Gly
|
|
XM_011534044.1:c.1043A>G
|
XP_011532346.1:p.Asp348Gly
|
|
XM_011534045.1:c.986A>G
|
XP_011532347.1:p.Asp329Gly
|
|
XM_011534043.2:c.1118A>G
|
XP_011532345.1:p.Asp373Gly
|
|
XM_011534045.3:c.986A>G
|
XP_011532347.1:p.Asp329Gly
|
|
XM_017007106.1:c.986A>G
|
XP_016862595.1:p.Asp329Gly
|
|
NM_003242.6:c.1091A>G
MANE Select
|
NP_003233.4:p.Asp364Gly
|
|