ENST00000295754.10:c.1385A>T
MANE Select
|
ENSP00000295754.5:p.Asn462Ile
|
|
ENST00000672866.1:n.2981A>T
|
|
|
ENST00000673203.1:n.263A>T
|
|
|
ENST00000295754.9:c.1385A>T
|
ENSP00000295754.5:p.Asn462Ile
|
|
ENST00000359013.4:c.1460A>T
|
ENSP00000351905.4:p.Asn487Ile
|
|
NM_001024847.2:c.1460A>T , LRG_779t1:c.1460A>T
|
NP_001020018.1:p.Asn487Ile
|
|
NM_003242.5:c.1385A>T
|
NP_003233.4:p.Asn462Ile
|
|
XM_011534043.1:c.1412A>T
|
XP_011532345.1:p.Asn471Ile
|
|
XM_011534044.1:c.1337A>T
|
XP_011532346.1:p.Asn446Ile
|
|
XM_011534045.1:c.1280A>T
|
XP_011532347.1:p.Asn427Ile
|
|
XM_011534043.2:c.1412A>T
|
XP_011532345.1:p.Asn471Ile
|
|
XM_011534045.3:c.1280A>T
|
XP_011532347.1:p.Asn427Ile
|
|
XM_017007106.1:c.1280A>T
|
XP_016862595.1:p.Asn427Ile
|
|
NM_003242.6:c.1385A>T
MANE Select
|
NP_003233.4:p.Asn462Ile
|
|