ENST00000646089.2:c.93+9023T>G
|
ENSP00000496197.1:n.93+9023T>G
|
|
ENST00000697624.1:n.200+9023T>G
|
|
|
ENST00000697625.1:c.93+9023T>G
|
ENSP00000513362.1:n.93+9023T>G
|
|
ENST00000697636.1:c.93+9023T>G
|
ENSP00000513366.1:n.93+9023T>G
|
|
ENST00000697637.1:c.93+9023T>G
|
ENSP00000513367.1:n.93+9023T>G
|
|
ENST00000697664.1:c.140+4859T>G
|
ENSP00000513389.1:n.140+4859T>G
|
|
ENST00000697665.1:c.93+9023T>G
|
ENSP00000513390.1:n.93+9023T>G
|
|
ENST00000697666.1:c.140+4859T>G
|
ENSP00000513391.1:n.140+4859T>G
|
|
ENST00000355622.8:c.1460T>G
MANE Select
|
ENSP00000363089.5:p.Phe487Cys
|
|
ENST00000394487.5:c.1340T>G
|
ENSP00000377997.4:p.Phe447Cys
|
|
ENST00000472304.2:c.*1194T>G
|
ENSP00000496429.1:n.*1194T>G
|
|
ENST00000642985.1:c.260+4859T>G
|
ENSP00000493686.1:n.260+4859T>G
|
|
ENST00000646089.1:c.93+9023T>G
|
ENSP00000496197.1:n.93+9023T>G
|
|
ENST00000665764.1:c.93+9023T>G
|
ENSP00000499745.1:n.93+9023T>G
|
|
ENST00000355622.6:c.1460T>G
|
ENSP00000363089.5:p.Phe487Cys
|
|
ENST00000394487.4:c.1340T>G
|
ENSP00000377997.4:p.Phe447Cys
|
|
ENST00000472304.1:n.1377T>G
|
|
|
NM_003266.3:c.1340T>G
|
NP_003257.1:p.Phe447Cys
|
|
NM_138554.4:c.1460T>G
|
NP_612564.1:p.Phe487Cys
|
|
NM_138557.2:c.860T>G
|
NP_612567.1:p.Phe287Cys
|
|
NM_138554.5:c.1460T>G
MANE Select
|
NP_612564.1:p.Phe487Cys
|
|
NM_003266.4:c.1340T>G
|
NP_003257.1:p.Phe447Cys
|
|
NM_138557.3:c.860T>G
|
NP_612567.1:p.Phe287Cys
|
|