ENST00000290866.10:c.352C>G
MANE Select
|
ENSP00000290866.4:p.Arg118Gly
|
|
ENST00000290866.9:c.352C>G
|
ENSP00000290866.4:p.Arg118Gly
|
|
ENST00000428043.5:c.352C>G
|
ENSP00000397593.2:p.Arg118Gly
|
|
ENST00000579462.1:n.377C>G
|
|
|
ENST00000580318.1:n.541C>G
|
|
|
ENST00000582627.1:c.352C>G
|
ENSP00000462280.1:p.Arg118Gly
|
|
ENST00000582678.5:c.352C>G
|
ENSP00000462995.1:p.Arg118Gly
|
|
ENST00000583336.5:n.386C>G
|
|
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ENST00000584529.5:n.386C>G
|
|
|
NM_000789.3:c.352C>G
|
NP_000780.1:p.Arg118Gly
|
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XM_005257110.1:c.-104C>G
|
XP_005257167.1:n.-104C>G
|
|
NM_000789.4:c.352C>G
MANE Select
|
NP_000780.1:p.Arg118Gly
|
|
NM_001382700.1:c.117C>G
|
NP_001369629.1:p.Cys39Trp
|
|
NM_001382701.1:c.-263C>G
|
NP_001369630.1:n.-263C>G
|
|