ENST00000440970.6:c.3913A>C
|
ENSP00000407914.2:p.Asn1305His
|
|
ENST00000570206.2:c.3622A>C
|
ENSP00000456777.2:p.Asn1208His
|
|
ENST00000685868.1:c.3913A>C
|
ENSP00000509873.1:p.Asn1305His
|
|
ENST00000251020.9:c.3913A>C
MANE Select
|
ENSP00000251020.4:p.Asn1305His
|
|
ENST00000251020.8:c.3913A>C
|
ENSP00000251020.4:p.Asn1305His
|
|
ENST00000440970.5:c.3622A>C
|
ENSP00000407914.1:p.Asn1208His
|
|
ENST00000566102.1:c.455A>C
|
ENSP00000455582.1:n.455A>C
|
|
NM_001127892.1:c.3622A>C
|
NP_001121364.1:p.Asn1208His
|
|
NM_002968.2:c.3913A>C , LRG_674t1:c.3913A>C
|
NP_002959.2:p.Asn1305His
|
|
XM_006721241.2:c.3913A>C
|
XP_006721304.1:p.Asn1305His
|
|
XM_011523254.1:c.3913A>C
|
XP_011521556.1:p.Asn1305His
|
|
XM_011523255.1:c.3913A>C
|
XP_011521557.1:p.Asn1305His
|
|
NM_002968.3:c.3913A>C
MANE Select
|
NP_002959.2:p.Asn1305His
|
|
NM_001127892.2:c.3622A>C
|
NP_001121364.1:p.Asn1208His
|
|