ENST00000703162.1:n.176A>C
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ENST00000281043.4:c.827A>C
MANE Select
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ENSP00000281043.3:p.Glu276Ala
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ENST00000638417.1:c.194A>C
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ENSP00000491476.1:p.Glu65Ala
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ENST00000281043.3:c.827A>C
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ENSP00000281043.3:p.Glu276Ala
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NM_001293228.1:c.827A>C
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NP_001280157.1:p.Glu276Ala
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NM_001293231.1:c.194A>C
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NP_001280160.1:p.Glu65Ala
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NM_001293233.1:c.*762A>C
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NP_001280162.1:n.*762A>C
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NM_005378.5:c.827A>C
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NP_005369.2:p.Glu276Ala
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NM_005378.6:c.827A>C
MANE Select
|
NP_005369.2:p.Glu276Ala
|
|
NM_001293228.2:c.827A>C
|
NP_001280157.1:p.Glu276Ala
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|
NM_001293231.2:c.194A>C
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NP_001280160.1:p.Glu65Ala
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|
NM_001293233.2:c.*762A>C
|
NP_001280162.1:n.*762A>C
|
|