ENST00000344265.8:c.868A>C
|
ENSP00000342931.3:p.Asn290His
|
|
ENST00000350375.7:c.790A>C
MANE Select
|
ENSP00000263781.2:p.Asn264His
|
|
ENST00000344265.7:c.868A>C
|
ENSP00000342931.3:p.Asn290His
|
|
ENST00000350375.6:c.790A>C
|
ENSP00000263781.2:p.Asn264His
|
|
ENST00000560656.1:c.564A>C
|
ENSP00000452610.1:n.564A>C
|
|
ENST00000561167.5:c.565A>C
|
ENSP00000454072.1:p.Asn189His
|
|
NM_000306.3:c.790A>C
|
NP_000297.1:p.Asn264His
|
|
NM_001122757.2:c.868A>C
|
NP_001116229.1:p.Asn290His
|
|
NM_000306.4:c.790A>C
MANE Select
|
NP_000297.1:p.Asn264His
|
|
NM_001122757.3:c.868A>C
|
NP_001116229.1:p.Asn290His
|
|