ENST00000295754.10:c.724C>G
MANE Select
|
ENSP00000295754.5:p.Leu242Val
|
|
ENST00000672866.1:n.2320C>G
|
|
|
ENST00000295754.9:c.724C>G
|
ENSP00000295754.5:p.Leu242Val
|
|
ENST00000359013.4:c.799C>G
|
ENSP00000351905.4:p.Leu267Val
|
|
NM_001024847.2:c.799C>G , LRG_779t1:c.799C>G
|
NP_001020018.1:p.Leu267Val
|
|
NM_003242.5:c.724C>G
|
NP_003233.4:p.Leu242Val
|
|
XM_011534043.1:c.751C>G
|
XP_011532345.1:p.Leu251Val
|
|
XM_011534044.1:c.676C>G
|
XP_011532346.1:p.Leu226Val
|
|
XM_011534045.1:c.619C>G
|
XP_011532347.1:p.Leu207Val
|
|
XM_011534043.2:c.751C>G
|
XP_011532345.1:p.Leu251Val
|
|
XM_011534045.3:c.619C>G
|
XP_011532347.1:p.Leu207Val
|
|
XM_017007106.1:c.619C>G
|
XP_016862595.1:p.Leu207Val
|
|
NM_003242.6:c.724C>G
MANE Select
|
NP_003233.4:p.Leu242Val
|
|