ENST00000354638.8:c.2269C>A
MANE Select
|
ENSP00000346659.3:p.His757Asn
|
|
ENST00000353809.9:c.2197C>A
|
ENSP00000261276.8:p.His733Asn
|
|
ENST00000354638.7:c.2269C>A
|
ENSP00000346659.3:p.His757Asn
|
|
NM_000275.2:c.2269C>A
|
NP_000266.2:p.His757Asn
|
|
NM_001300984.1:c.2197C>A
|
NP_001287913.1:p.His733Asn
|
|
XM_011521639.1:c.2335C>A
|
XP_011519941.1:p.His779Asn
|
|
XM_011521640.1:c.2311C>A
|
XP_011519942.1:p.His771Asn
|
|
XM_011521641.1:c.2293C>A
|
XP_011519943.1:p.His765Asn
|
|
XM_011521642.1:c.2263C>A
|
XP_011519944.1:p.His755Asn
|
|
XM_011521643.1:c.2221C>A
|
XP_011519945.1:p.His741Asn
|
|
XM_011521644.1:c.2197C>A
|
XP_011519946.1:p.His733Asn
|
|
XM_011521645.1:c.2128C>A
|
XP_011519947.1:p.His710Asn
|
|
XM_011521640.2:c.2311C>A
|
XP_011519942.1:p.His771Asn
|
|
XM_017022255.1:c.2335C>A
|
XP_016877744.1:p.His779Asn
|
|
XM_017022256.1:c.2293C>A
|
XP_016877745.1:p.His765Asn
|
|
XM_017022257.1:c.2263C>A
|
XP_016877746.1:p.His755Asn
|
|
XM_017022258.1:c.2293C>A
|
XP_016877747.1:p.His765Asn
|
|
XM_017022259.1:c.2221C>A
|
XP_016877748.1:p.His741Asn
|
|
XM_017022260.1:c.2197C>A
|
XP_016877749.1:p.His733Asn
|
|
XM_017022261.1:c.2140C>A
|
XP_016877750.1:p.His714Asn
|
|
XM_017022262.1:c.2268+19703C>A
|
XP_016877751.1:n.2268+19703C>A
|
|
XM_017022263.1:c.2128C>A
|
XP_016877752.1:p.His710Asn
|
|
XM_017022264.1:c.2128C>A
|
XP_016877753.1:p.His710Asn
|
|
NM_000275.3:c.2269C>A
MANE Select
|
NP_000266.2:p.His757Asn
|
|
NM_001300984.2:c.2197C>A
|
NP_001287913.1:p.His733Asn
|
|