ENST00000354638.8:c.2260A>C
MANE Select
|
ENSP00000346659.3:p.Asn754His
|
|
ENST00000353809.9:c.2188A>C
|
ENSP00000261276.8:p.Asn730His
|
|
ENST00000354638.7:c.2260A>C
|
ENSP00000346659.3:p.Asn754His
|
|
NM_000275.2:c.2260A>C
|
NP_000266.2:p.Asn754His
|
|
NM_001300984.1:c.2188A>C
|
NP_001287913.1:p.Asn730His
|
|
XM_011521639.1:c.2326A>C
|
XP_011519941.1:p.Asn776His
|
|
XM_011521640.1:c.2302A>C
|
XP_011519942.1:p.Asn768His
|
|
XM_011521641.1:c.2284A>C
|
XP_011519943.1:p.Asn762His
|
|
XM_011521642.1:c.2254A>C
|
XP_011519944.1:p.Asn752His
|
|
XM_011521643.1:c.2212A>C
|
XP_011519945.1:p.Asn738His
|
|
XM_011521644.1:c.2188A>C
|
XP_011519946.1:p.Asn730His
|
|
XM_011521645.1:c.2119A>C
|
XP_011519947.1:p.Asn707His
|
|
XM_011521640.2:c.2302A>C
|
XP_011519942.1:p.Asn768His
|
|
XM_017022255.1:c.2326A>C
|
XP_016877744.1:p.Asn776His
|
|
XM_017022256.1:c.2284A>C
|
XP_016877745.1:p.Asn762His
|
|
XM_017022257.1:c.2254A>C
|
XP_016877746.1:p.Asn752His
|
|
XM_017022258.1:c.2284A>C
|
XP_016877747.1:p.Asn762His
|
|
XM_017022259.1:c.2212A>C
|
XP_016877748.1:p.Asn738His
|
|
XM_017022260.1:c.2188A>C
|
XP_016877749.1:p.Asn730His
|
|
XM_017022261.1:c.2131A>C
|
XP_016877750.1:p.Asn711His
|
|
XM_017022262.1:c.2268+19694A>C
|
XP_016877751.1:n.2268+19694A>C
|
|
XM_017022263.1:c.2119A>C
|
XP_016877752.1:p.Asn707His
|
|
XM_017022264.1:c.2119A>C
|
XP_016877753.1:p.Asn707His
|
|
NM_000275.3:c.2260A>C
MANE Select
|
NP_000266.2:p.Asn754His
|
|
NM_001300984.2:c.2188A>C
|
NP_001287913.1:p.Asn730His
|
|