ENST00000642683.1:c.694T>A
|
ENSP00000495376.1:p.Tyr232Asn
|
|
ENST00000643672.1:c.691T>A
|
ENSP00000494532.1:p.Tyr231Asn
|
|
ENST00000645280.1:c.688T>A
|
ENSP00000496690.1:p.Tyr230Asn
|
|
ENST00000648579.1:c.*39T>A
|
ENSP00000497638.1:n.*39T>A
|
|
ENST00000650617.1:c.742T>A
MANE Select
|
ENSP00000497532.1:p.Tyr248Asn
|
|
ENST00000273158.8:c.742T>A
|
ENSP00000273158.3:p.Tyr248Asn
|
|
NM_017875.2:c.742T>A
|
NP_060345.2:p.Tyr248Asn
|
|
XM_006713214.1:c.730T>A
|
XP_006713277.1:p.Tyr244Asn
|
|
XM_011533869.1:c.724T>A
|
XP_011532171.1:p.Tyr242Asn
|
|
XM_011533870.1:c.691T>A
|
XP_011532172.1:p.Tyr231Asn
|
|
XM_011533871.1:c.562T>A
|
XP_011532173.1:p.Tyr188Asn
|
|
NM_001354798.1:c.626-1872T>A
|
NP_001341727.1:n.626-1872T>A
|
|
NM_017875.4:c.742T>A
MANE Select
|
NP_060345.2:p.Tyr248Asn
|
|
XM_006713214.2:c.730T>A
|
XP_006713277.1:p.Tyr244Asn
|
|
XM_011533869.2:c.724T>A
|
XP_011532171.1:p.Tyr242Asn
|
|
XM_024453611.1:c.688T>A
|
XP_024309379.1:p.Tyr230Asn
|
|
NM_001354798.2:c.626-1872T>A
|
NP_001341727.1:n.626-1872T>A
|
|