ENST00000481739.2:c.376A>C
MANE Select
|
ENSP00000419692.1:p.Asn126His
|
|
ENST00000672570.1:c.295A>C
|
ENSP00000500402.1:p.Asn99His
|
|
ENST00000356384.4:n.786A>C
|
|
|
ENST00000481739.1:c.376A>C
|
ENSP00000419692.1:p.Asn126His
|
|
NM_001291920.1:c.295A>C
|
NP_001278849.1:p.Asn99His
|
|
NM_001291921.1:c.85A>C
|
NP_001278850.1:p.Asn29His
|
|
NM_002957.5:c.376A>C
|
NP_002948.1:p.Asn126His
|
|
NM_002957.6:c.376A>C
MANE Select
|
NP_002948.1:p.Asn126His
|
|
NM_001291921.2:c.85A>C
|
NP_001278850.1:p.Asn29His
|
|
NM_001291920.2:c.295A>C
|
NP_001278849.1:p.Asn99His
|
|