ENST00000269228.10:c.3628A>T
MANE Select
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ENSP00000269228.4:p.Ile1210Phe
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ENST00000269228.9:c.3628A>T
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ENSP00000269228.4:p.Ile1210Phe
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ENST00000586150.5:c.383A>T
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|
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ENST00000587163.1:n.152A>T
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|
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ENST00000588867.1:n.1311A>T
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|
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ENST00000590723.5:c.37A>T
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ENSP00000464755.1:p.Ile13Phe
|
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ENST00000591051.1:c.2706A>T
|
|
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ENST00000591107.6:c.305A>T
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NM_000271.4:c.3628A>T
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NP_000262.2:p.Ile1210Phe
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XM_005258277.1:c.3679A>T
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XP_005258334.1:p.Ile1227Phe
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XM_005258278.3:c.3679A>T
|
XP_005258335.1:p.Ile1227Phe
|
|
XM_005258279.1:c.3628A>T
|
XP_005258336.1:p.Ile1210Phe
|
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XM_006722479.2:c.3679A>T
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XP_006722542.1:p.Ile1227Phe
|
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XM_011526015.1:c.3214A>T
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XP_011524317.1:p.Ile1072Phe
|
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XM_005258278.5:c.3679A>T
|
XP_005258335.1:p.Ile1227Phe
|
|
XM_005258279.2:c.3628A>T
|
XP_005258336.1:p.Ile1210Phe
|
|
XM_006722479.3:c.3679A>T
|
XP_006722542.1:p.Ile1227Phe
|
|
XM_017025784.1:c.3679A>T
|
XP_016881273.1:p.Ile1227Phe
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|
XM_017025785.1:c.3679A>T
|
XP_016881274.1:p.Ile1227Phe
|
|
XM_017025786.1:c.3628A>T
|
XP_016881275.1:p.Ile1210Phe
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|
XM_017025787.1:c.3628A>T
|
XP_016881276.1:p.Ile1210Phe
|
|
NM_000271.5:c.3628A>T
MANE Select
|
NP_000262.2:p.Ile1210Phe
|
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