ENST00000642496.1:c.3999C>T
|
|
|
ENST00000644397.2:c.5140C>T
MANE Select
|
ENSP00000495195.1:p.His1714Tyr
|
|
ENST00000373965.6:c.4951C>T
|
ENSP00000363076.3:p.His1651Tyr
|
|
ENST00000414778.5:c.4948C>T
|
ENSP00000410304.2:p.His1650Tyr
|
|
ENST00000495484.5:c.1168C>T
|
ENSP00000480780.1:p.His390Tyr
|
|
ENST00000614895.4:c.4963C>T
|
ENSP00000478512.1:p.His1655Tyr
|
|
ENST00000616114.4:c.4945C>T
|
ENSP00000483745.1:p.His1649Tyr
|
|
ENST00000618301.4:c.1300C>T
|
ENSP00000482780.1:p.His434Tyr
|
|
ENST00000621708.4:c.4966C>T
|
ENSP00000484454.1:p.His1656Tyr
|
|
NM_001142771.1:c.4966C>T
|
NP_001136243.1:p.His1656Tyr
|
|
NM_001142772.1:c.4951C>T
|
NP_001136244.1:p.His1651Tyr
|
|
NM_001354420.1:c.4945C>T
|
NP_001341349.1:p.His1649Tyr
|
|
NM_001354429.1:c.5074C>T
|
NP_001341358.1:p.His1692Tyr
|
|
XR_001747192.2:n.11432C>T
|
|
|
XR_001747193.2:n.11423C>T
|
|
|
NM_001142771.2:c.4966C>T
|
NP_001136243.1:p.His1656Tyr
|
|
NM_001142772.2:c.4951C>T
|
NP_001136244.1:p.His1651Tyr
|
|
NM_001354420.2:c.4945C>T
|
NP_001341349.1:p.His1649Tyr
|
|
NM_001354429.2:c.5074C>T
|
NP_001341358.1:p.His1692Tyr
|
|
NM_001384140.1:c.5140C>T
MANE Select
|
NP_001371069.1:p.His1714Tyr
|
|