ENST00000290866.10:c.3873C>T
MANE Select
|
ENSP00000290866.4:p.His1291=
|
|
ENST00000290863.10:c.2151C>T
|
ENSP00000290863.6:p.His717=
|
|
ENST00000290866.9:c.3873C>T
|
ENSP00000290866.4:p.His1291=
|
|
ENST00000413513.7:c.2028C>T
|
ENSP00000392247.3:p.His676=
|
|
ENST00000428043.5:c.*295C>T
|
ENSP00000397593.2:n.*295C>T
|
|
ENST00000577647.2:c.1969+333C>T
|
ENSP00000464149.1:n.1969+333C>T
|
|
ENST00000578839.5:c.*1628C>T
|
ENSP00000462110.2:n.*1628C>T
|
|
ENST00000579314.5:c.*1602C>T
|
ENSP00000462599.1:n.*1602C>T
|
|
NM_000789.3:c.3873C>T
|
NP_000780.1:p.His1291=
|
|
NM_001178057.1:c.2028C>T
|
NP_001171528.1:p.His676=
|
|
NM_152830.2:c.2151C>T
|
NP_690043.1:p.His717=
|
|
XM_005257110.1:c.3324C>T
|
XP_005257167.1:p.His1108=
|
|
XM_006721737.2:c.2211C>T
|
XP_006721800.2:p.His737=
|
|
XM_006721737.3:c.2211C>T
|
XP_006721800.2:p.His737=
|
|
NM_000789.4:c.3873C>T
MANE Select
|
NP_000780.1:p.His1291=
|
|
NM_001178057.2:c.2028C>T
|
NP_001171528.1:p.His676=
|
|
NM_152830.3:c.2151C>T
|
NP_690043.1:p.His717=
|
|
NM_001382700.1:c.3306C>T
|
NP_001369629.1:p.His1102=
|
|
NM_001382701.1:c.3021C>T
|
NP_001369630.1:p.His1007=
|
|
NM_001382702.1:c.1488C>T
|
NP_001369631.1:p.His496=
|
|
NR_168483.1:n.2251C>T
|
|
|