ENST00000262367.10:c.6296C=
MANE Select
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ENSP00000262367.5:p.Ala2099=
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ENST00000262367.9:c.6296C=
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ENSP00000262367.5:p.Ala2099=
|
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ENST00000382070.7:c.6182C=
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ENSP00000371502.3:p.Ala2061=
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NM_001079846.1:c.6182C=
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NP_001073315.1:p.Ala2061=
|
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NM_004380.2:c.6296C=
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NP_004371.2:p.Ala2099=
|
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XM_005255124.3:c.6251C=
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XP_005255181.1:p.Ala2084=
|
|
XM_005255125.3:c.5879C=
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XP_005255182.1:p.Ala1960=
|
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XM_006720848.2:c.6035C=
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XP_006720911.1:p.Ala2012=
|
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XM_011522380.1:c.6242C=
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XP_011520682.1:p.Ala2081=
|
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XM_011522381.1:c.5543C=
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XP_011520683.1:p.Ala1848=
|
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XM_005255124.4:c.6251C=
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XP_005255181.1:p.Ala2084=
|
|
XM_005255125.4:c.5879C=
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XP_005255182.1:p.Ala1960=
|
|
XM_006720848.3:c.6035C=
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XP_006720911.1:p.Ala2012=
|
|
XM_011522381.2:c.5543C=
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XP_011520683.1:p.Ala1848=
|
|
XM_017022944.1:c.6290C=
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XP_016878433.1:p.Ala2097=
|
|
NM_004380.3:c.6296C=
MANE Select
|
NP_004371.2:p.Ala2099=
|
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