ENST00000299565.9:c.*623A>G
(CHRNA5)
MANE Select
|
ENSP00000299565.5:n.*623A>G
|
|
ENST00000348639.7:c.1390-685T>C
(CHRNA3)
|
ENSP00000267951.4:n.1390-685T>C
|
|
ENST00000559002.5:n.194-685T>C
(CHRNA3)
|
|
|
ENST00000559658.5:c.*162+38T>C
(CHRNA3)
|
ENSP00000452896.1:n.*162+38T>C
|
|
NM_000745.3:c.*623A>G
(CHRNA5)
|
NP_000736.2:n.*623A>G
|
|
NM_001166694.1:c.1390-685T>C
(CHRNA3)
|
NP_001160166.1:n.1390-685T>C
|
|
NM_001307945.1:c.*760A>G
(CHRNA5)
|
NP_001294874.1:n.*760A>G
|
|
NR_046313.1:n.2181+38T>C
(CHRNA3)
|
|
|
NM_001166694.2:c.1390-685T>C
(CHRNA3)
|
NP_001160166.1:n.1390-685T>C
|
|
NM_001307945.2:c.*760A>G
(CHRNA5)
|
NP_001294874.1:n.*760A>G
|
|
NR_046313.2:n.1882+38T>C
(CHRNA3)
|
|
|
NM_000745.4:c.*623A>G
(CHRNA5)
MANE Select
|
NP_000736.2:n.*623A>G
|
|
NM_001395171.1:c.*760A>G
(CHRNA5)
|
NP_001382100.1:n.*760A>G
|
|
NM_001395172.1:c.*623A>G
(CHRNA5)
|
NP_001382101.1:n.*623A>G
|
|
NM_001395173.1:c.*760A>G
(CHRNA5)
|
NP_001382102.1:n.*760A>G
|
|
NM_001395174.1:c.*760A>G
(CHRNA5)
|
NP_001382103.1:n.*760A>G
|
|
NM_001395175.1:c.*760A>G
(CHRNA5)
|
NP_001382104.1:n.*760A>G
|
|