ENST00000525341.2:c.683A>C
|
|
|
ENST00000528641.7:c.517A>C
|
ENSP00000434982.3:p.Asn173His
|
|
ENST00000529797.2:n.1218A>C
|
|
|
ENST00000682324.1:c.469-621A>C
|
ENSP00000508017.1:n.469-621A>C
|
|
ENST00000682659.1:c.337A>C
|
ENSP00000507351.1:p.Asn113His
|
|
ENST00000682699.1:c.706A>C
|
ENSP00000507935.1:p.Asn236His
|
|
ENST00000683237.1:c.706A>C
|
ENSP00000507343.1:p.Asn236His
|
|
ENST00000683856.1:c.529A>C
|
ENSP00000507979.1:p.Asn177His
|
|
ENST00000684006.1:c.706A>C
|
ENSP00000507269.1:p.Asn236His
|
|
ENST00000684657.1:c.526A>C
|
ENSP00000507961.1:p.Asn176His
|
|
ENST00000279146.8:c.706A>C
MANE Select
|
ENSP00000279146.3:p.Asn236His
|
|
ENST00000279146.7:c.706A>C
|
ENSP00000279146.3:p.Asn236His
|
|
ENST00000525341.1:c.358A>C
|
ENSP00000476993.1:p.Asn120His
|
|
ENST00000528641.6:c.517A>C
|
ENSP00000434982.2:p.Asn173His
|
|
NM_001302959.1:c.529A>C
|
NP_001289888.1:p.Asn177His
|
|
NM_001302960.1:c.706A>C
|
NP_001289889.1:p.Asn236His
|
|
NM_003977.3:c.706A>C
|
NP_003968.3:p.Asn236His
|
|
XM_024448761.1:c.706A>C
|
XP_024304529.1:p.Asn236His
|
|
NM_003977.4:c.706A>C
MANE Select
|
NP_003968.3:p.Asn236His
|
|
NM_001302960.2:c.706A>C
|
NP_001289889.1:p.Asn236His
|
|
NM_001302959.2:c.529A>C
|
NP_001289888.1:p.Asn177His
|
|