ENST00000642496.1:c.4053A>T
|
|
|
ENST00000644397.2:c.5194A>T
MANE Select
|
ENSP00000495195.1:p.Asn1732Tyr
|
|
ENST00000373965.6:c.5005A>T
|
ENSP00000363076.3:p.Asn1669Tyr
|
|
ENST00000414778.5:c.5002A>T
|
ENSP00000410304.2:p.Asn1668Tyr
|
|
ENST00000495484.5:c.1222A>T
|
ENSP00000480780.1:p.Asn408Tyr
|
|
ENST00000614895.4:c.5017A>T
|
ENSP00000478512.1:p.Asn1673Tyr
|
|
ENST00000616114.4:c.4999A>T
|
ENSP00000483745.1:p.Asn1667Tyr
|
|
ENST00000618301.4:c.1354A>T
|
ENSP00000482780.1:p.Asn452Tyr
|
|
ENST00000621708.4:c.5020A>T
|
ENSP00000484454.1:p.Asn1674Tyr
|
|
NM_001142771.1:c.5020A>T
|
NP_001136243.1:p.Asn1674Tyr
|
|
NM_001142772.1:c.5005A>T
|
NP_001136244.1:p.Asn1669Tyr
|
|
NM_001354420.1:c.4999A>T
|
NP_001341349.1:p.Asn1667Tyr
|
|
NM_001354429.1:c.5128A>T
|
NP_001341358.1:p.Asn1710Tyr
|
|
XR_001747192.2:n.11486A>T
|
|
|
XR_001747193.2:n.11477A>T
|
|
|
NM_001142771.2:c.5020A>T
|
NP_001136243.1:p.Asn1674Tyr
|
|
NM_001142772.2:c.5005A>T
|
NP_001136244.1:p.Asn1669Tyr
|
|
NM_001354420.2:c.4999A>T
|
NP_001341349.1:p.Asn1667Tyr
|
|
NM_001354429.2:c.5128A>T
|
NP_001341358.1:p.Asn1710Tyr
|
|
NM_001384140.1:c.5194A>T
MANE Select
|
NP_001371069.1:p.Asn1732Tyr
|
|