ENST00000290866.10:c.288C>G
MANE Select
|
ENSP00000290866.4:p.Ala96=
|
|
ENST00000290866.9:c.288C>G
|
ENSP00000290866.4:p.Ala96=
|
|
ENST00000428043.5:c.288C>G
|
ENSP00000397593.2:p.Ala96=
|
|
ENST00000579462.1:n.313C>G
|
|
|
ENST00000580318.1:n.477C>G
|
|
|
ENST00000582627.1:c.288C>G
|
ENSP00000462280.1:p.Ala96=
|
|
ENST00000582678.5:c.288C>G
|
ENSP00000462995.1:p.Ala96=
|
|
ENST00000583336.5:n.322C>G
|
|
|
ENST00000584529.5:n.322C>G
|
|
|
NM_000789.3:c.288C>G
|
NP_000780.1:p.Ala96=
|
|
XM_005257110.1:c.-168C>G
|
XP_005257167.1:n.-168C>G
|
|
NM_000789.4:c.288C>G
MANE Select
|
NP_000780.1:p.Ala96=
|
|
NM_001382700.1:c.53C>G
|
NP_001369629.1:p.Pro18Arg
|
|
NM_001382701.1:c.-327C>G
|
NP_001369630.1:n.-327C>G
|
|