ENST00000395715.8:c.3415C>A
MANE Select
|
ENSP00000379065.3:p.His1139Asn
|
|
ENST00000640765.1:c.3376C>A
|
ENSP00000492037.1:p.His1126Asn
|
|
ENST00000220888.9:c.3376C>A
|
ENSP00000220888.5:p.His1126Asn
|
|
ENST00000395715.7:c.3415C>A
|
ENSP00000379065.3:p.His1139Asn
|
|
ENST00000518018.1:c.749C>A
|
|
|
ENST00000519076.5:c.2638C>A
|
ENSP00000428910.1:p.His880Asn
|
|
ENST00000520276.5:c.3388C>A
|
ENSP00000428680.1:p.His1130Asn
|
|
NM_001282902.2:c.3388C>A
|
NP_001269831.1:p.His1130Asn
|
|
NM_001282903.2:c.3394C>A
|
NP_001269832.1:p.His1132Asn
|
|
NM_014112.4:c.3415C>A
|
NP_054831.2:p.His1139Asn
|
|
XM_005251049.2:c.3376C>A
|
XP_005251106.1:p.His1126Asn
|
|
XM_006716625.1:c.3415C>A
|
XP_006716688.1:p.His1139Asn
|
|
XM_011517264.1:c.3415C>A
|
XP_011515566.1:p.His1139Asn
|
|
XM_011517265.1:c.3415C>A
|
XP_011515567.1:p.His1139Asn
|
|
XM_011517266.1:c.3415C>A
|
XP_011515568.1:p.His1139Asn
|
|
XM_011517267.1:c.3394C>A
|
XP_011515569.1:p.His1132Asn
|
|
XM_011517268.1:c.3376C>A
|
XP_011515570.1:p.His1126Asn
|
|
NM_001330599.1:c.3376C>A
|
NP_001317528.1:p.His1126Asn
|
|
XM_011517264.2:c.3415C>A
|
XP_011515566.1:p.His1139Asn
|
|
XM_011517266.3:c.3415C>A
|
XP_011515568.1:p.His1139Asn
|
|
XM_011517268.2:c.3376C>A
|
XP_011515570.1:p.His1126Asn
|
|
NM_001282902.3:c.3388C>A
|
NP_001269831.1:p.His1130Asn
|
|
NM_001282903.3:c.3394C>A
|
NP_001269832.1:p.His1132Asn
|
|
NM_001330599.2:c.3376C>A
|
NP_001317528.1:p.His1126Asn
|
|
NM_014112.5:c.3415C>A
MANE Select
|
NP_054831.2:p.His1139Asn
|
|