ENST00000295754.10:c.1551G>A
MANE Select
|
ENSP00000295754.5:p.Leu517=
|
|
ENST00000672050.1:n.435G>A
|
|
|
ENST00000672866.1:n.3147G>A
|
|
|
ENST00000673203.1:n.429G>A
|
|
|
ENST00000295754.9:c.1551G>A
|
ENSP00000295754.5:p.Leu517=
|
|
ENST00000359013.4:c.1626G>A
|
ENSP00000351905.4:p.Leu542=
|
|
NM_001024847.2:c.1626G>A , LRG_779t1:c.1626G>A
|
NP_001020018.1:p.Leu542=
|
|
NM_003242.5:c.1551G>A
|
NP_003233.4:p.Leu517=
|
|
XM_011534043.1:c.1578G>A
|
XP_011532345.1:p.Leu526=
|
|
XM_011534044.1:c.1503G>A
|
XP_011532346.1:p.Leu501=
|
|
XM_011534045.1:c.1446G>A
|
XP_011532347.1:p.Leu482=
|
|
XM_011534043.2:c.1578G>A
|
XP_011532345.1:p.Leu526=
|
|
XM_011534045.3:c.1446G>A
|
XP_011532347.1:p.Leu482=
|
|
XM_017007106.1:c.1446G>A
|
XP_016862595.1:p.Leu482=
|
|
NM_003242.6:c.1551G>A
MANE Select
|
NP_003233.4:p.Leu517=
|
|