ENST00000290866.10:c.340G>C
MANE Select
|
ENSP00000290866.4:p.Asp114His
|
|
ENST00000290866.9:c.340G>C
|
ENSP00000290866.4:p.Asp114His
|
|
ENST00000428043.5:c.340G>C
|
ENSP00000397593.2:p.Asp114His
|
|
ENST00000579462.1:n.365G>C
|
|
|
ENST00000580318.1:n.529G>C
|
|
|
ENST00000582627.1:c.340G>C
|
ENSP00000462280.1:p.Asp114His
|
|
ENST00000582678.5:c.340G>C
|
ENSP00000462995.1:p.Asp114His
|
|
ENST00000583336.5:n.374G>C
|
|
|
ENST00000584529.5:n.374G>C
|
|
|
NM_000789.3:c.340G>C
|
NP_000780.1:p.Asp114His
|
|
XM_005257110.1:c.-116G>C
|
XP_005257167.1:n.-116G>C
|
|
NM_000789.4:c.340G>C
MANE Select
|
NP_000780.1:p.Asp114His
|
|
NM_001382700.1:c.105G>C
|
NP_001369629.1:p.Arg35=
|
|
NM_001382701.1:c.-275G>C
|
NP_001369630.1:n.-275G>C
|
|