ENST00000290866.10:c.1167C>G
MANE Select
|
ENSP00000290866.4:p.His389Gln
|
|
ENST00000290866.9:c.1167C>G
|
ENSP00000290866.4:p.His389Gln
|
|
ENST00000428043.5:c.1167C>G
|
ENSP00000397593.2:p.His389Gln
|
|
ENST00000582678.5:c.*566C>G
|
ENSP00000462995.1:n.*566C>G
|
|
ENST00000584529.5:n.1201C>G
|
|
|
NM_000789.3:c.1167C>G
|
NP_000780.1:p.His389Gln
|
|
XM_005257110.1:c.618C>G
|
XP_005257167.1:p.His206Gln
|
|
NM_000789.4:c.1167C>G
MANE Select
|
NP_000780.1:p.His389Gln
|
|
NM_001382700.1:c.600C>G
|
NP_001369629.1:p.His200Gln
|
|
NM_001382701.1:c.315C>G
|
NP_001369630.1:p.His105Gln
|
|