ENST00000377873.8:c.803A>T
MANE Select
|
ENSP00000367104.3:p.Asn268Ile
|
|
ENST00000536626.7:c.386A>T
|
ENSP00000442522.1:p.Asn129Ile
|
|
ENST00000377868.6:c.428A>T
|
ENSP00000367099.2:p.Asn143Ile
|
|
ENST00000377873.7:c.803A>T
|
ENSP00000367104.3:p.Asn268Ile
|
|
ENST00000536626.5:c.386A>T
|
ENSP00000442522.1:p.Asn129Ile
|
|
NM_001161705.1:c.428A>T
|
NP_001155177.1:p.Asn143Ile
|
|
NM_001195.4:c.803A>T
|
NP_001186.1:p.Asn268Ile
|
|
NM_001278606.1:c.386A>T
|
NP_001265535.1:p.Asn129Ile
|
|
NM_001278607.1:c.470A>T
|
NP_001265536.1:p.Asn157Ile
|
|
NM_001278608.1:c.386A>T
|
NP_001265537.1:p.Asn129Ile
|
|
XM_011529312.1:c.386A>T
|
XP_011527614.1:p.Asn129Ile
|
|
XM_017028005.2:c.695A>T
|
XP_016883494.1:p.Asn232Ile
|
|
NM_001195.5:c.803A>T
MANE Select
|
NP_001186.1:p.Asn268Ile
|
|
NM_001161705.2:c.428A>T
|
NP_001155177.1:p.Asn143Ile
|
|
NM_001278606.2:c.386A>T
|
NP_001265535.1:p.Asn129Ile
|
|
NM_001278607.2:c.470A>T
|
NP_001265536.1:p.Asn157Ile
|
|
NM_001278608.2:c.386A>T
|
NP_001265537.1:p.Asn129Ile
|
|