NM_001289162.2:c.1317T>G
MANE Select
|
NP_001276091.1:p.Ile439Met
|
ENST00000360716.8:c.1317T>G
MANE Select
|
ENSP00000353942.3:p.Ile439Met
|
NM_001289162.1:c.1317T>G
|
NP_001276091.1:p.Ile439Met
|
NM_001289163.1:c.1122T>G
|
NP_001276092.1:p.Ile374Met
|
NM_001289163.2:c.1122T>G
|
NP_001276092.1:p.Ile374Met
|
NM_032269.5:c.1317T>G
|
NP_115645.4:p.Ile439Met
|
NM_032269.6:c.1317T>G
|
NP_115645.4:p.Ile439Met
|
ENST00000336825.12:c.1122T>G
|
ENSP00000338938.8:p.Ile374Met
|
ENST00000360716.7:c.1317T>G
|
ENSP00000353942.3:p.Ile439Met
|
ENST00000394337.8:c.1317T>G
|
ENSP00000377869.4:p.Ile439Met
|
ENST00000562250.1:c.86T>G
|
|
XM_011523377.1:c.1280-252T>G
|
XP_011521679.1:n.1280-252T>G
|
XM_011523378.1:c.1122T>G
|
XP_011521680.1:p.Ile374Met
|