ENST00000290866.10:c.1128G>C
MANE Select
|
ENSP00000290866.4:p.Gln376His
|
|
ENST00000290866.9:c.1128G>C
|
ENSP00000290866.4:p.Gln376His
|
|
ENST00000428043.5:c.1128G>C
|
ENSP00000397593.2:p.Gln376His
|
|
ENST00000582678.5:c.*527G>C
|
ENSP00000462995.1:n.*527G>C
|
|
ENST00000584529.5:n.1162G>C
|
|
|
NM_000789.3:c.1128G>C
|
NP_000780.1:p.Gln376His
|
|
XM_005257110.1:c.579G>C
|
XP_005257167.1:p.Gln193His
|
|
NM_000789.4:c.1128G>C
MANE Select
|
NP_000780.1:p.Gln376His
|
|
NM_001382700.1:c.561G>C
|
NP_001369629.1:p.Gln187His
|
|
NM_001382701.1:c.276G>C
|
NP_001369630.1:p.Gln92His
|
|