ENST00000295754.10:c.556T>A
MANE Select
|
ENSP00000295754.5:p.Phe186Ile
|
|
ENST00000672866.1:n.2152T>A
|
|
|
ENST00000295754.9:c.556T>A
|
ENSP00000295754.5:p.Phe186Ile
|
|
ENST00000359013.4:c.631T>A
|
ENSP00000351905.4:p.Phe211Ile
|
|
NM_001024847.2:c.631T>A , LRG_779t1:c.631T>A
|
NP_001020018.1:p.Phe211Ile
|
|
NM_003242.5:c.556T>A
|
NP_003233.4:p.Phe186Ile
|
|
XM_011534043.1:c.583T>A
|
XP_011532345.1:p.Phe195Ile
|
|
XM_011534044.1:c.508T>A
|
XP_011532346.1:p.Phe170Ile
|
|
XM_011534045.1:c.451T>A
|
XP_011532347.1:p.Phe151Ile
|
|
XM_011534043.2:c.583T>A
|
XP_011532345.1:p.Phe195Ile
|
|
XM_011534045.3:c.451T>A
|
XP_011532347.1:p.Phe151Ile
|
|
XM_017007106.1:c.451T>A
|
XP_016862595.1:p.Phe151Ile
|
|
NM_003242.6:c.556T>A
MANE Select
|
NP_003233.4:p.Phe186Ile
|
|