ENST00000563588.6:c.555A>G
MANE Select
|
ENSP00000455607.1:p.Arg185=
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|
ENST00000328273.11:c.555A>G
|
ENSP00000329968.7:p.Arg185=
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|
ENST00000424889.7:c.555A>G
|
ENSP00000388571.3:p.Arg185=
|
|
ENST00000561712.1:c.229A>G
|
|
|
ENST00000563588.5:c.555A>G
|
ENSP00000455607.1:p.Arg185=
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|
ENST00000563913.5:n.888A>G
|
|
|
ENST00000564838.5:n.929A>G
|
|
|
ENST00000565897.5:c.555A>G
|
ENSP00000457359.1:p.Arg185=
|
|
ENST00000565924.5:c.555A>G
|
ENSP00000455091.1:p.Arg185=
|
|
ENST00000569684.1:n.967A>G
|
|
|
NM_000294.2:c.555A>G
|
NP_000285.1:p.Arg185=
|
|
NM_001172432.1:c.555A>G
|
NP_001165903.1:p.Arg185=
|
|
NM_000294.3:c.555A>G
MANE Select
|
NP_000285.1:p.Arg185=
|
|
NM_001172432.2:c.555A>G
|
NP_001165903.1:p.Arg185=
|
|