ENST00000435881.7:c.710A>G
MANE Select
|
ENSP00000416627.1:p.His237Arg
|
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ENST00000246912.8:c.872A>G
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ENSP00000246912.3:p.His291Arg
|
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ENST00000346833.8:c.620A>G
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ENSP00000320913.3:p.His207Arg
|
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ENST00000435881.6:c.710A>G
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ENSP00000416627.1:p.His237Arg
|
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ENST00000585403.5:n.917A>G
|
|
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ENST00000588320.1:n.1186A>G
|
|
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ENST00000590050.5:n.876A>G
|
|
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NM_170607.2:c.872A>G
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NP_733752.1:p.His291Arg
|
|
NM_198204.1:c.710A>G
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NP_937847.1:p.His237Arg
|
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NM_198205.1:c.620A>G
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NP_937848.1:p.His207Arg
|
|
NM_198204.2:c.710A>G
MANE Select
|
NP_937847.1:p.His237Arg
|
|
NM_170607.3:c.872A>G
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NP_733752.1:p.His291Arg
|
|
NM_198205.2:c.620A>G
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NP_937848.1:p.His207Arg
|
|