ENST00000299314.12:c.1397G>C
MANE Select
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ENSP00000299314.7:p.Gly466Ala
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ENST00000299314.11:c.1397G>C
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ENSP00000299314.7:p.Gly466Ala
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ENST00000549940.5:c.1397G>C
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ENSP00000449150.1:p.Gly466Ala
|
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ENST00000552009.1:n.56G>C
|
|
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NM_024312.4:c.1397G>C
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NP_077288.2:p.Gly466Ala
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XM_006719593.2:c.1397G>C
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XP_006719656.1:p.Gly466Ala
|
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XM_011538731.1:c.1316G>C
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XP_011537033.1:p.Gly439Ala
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XM_006719593.3:c.1397G>C
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XP_006719656.1:p.Gly466Ala
|
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XM_011538731.2:c.1316G>C
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XP_011537033.1:p.Gly439Ala
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XM_017019961.1:c.1181G>C
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XP_016875450.1:p.Gly394Ala
|
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XM_017019962.2:c.170G>C
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XP_016875451.1:p.Gly57Ala
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NM_024312.5:c.1397G>C
MANE Select
|
NP_077288.2:p.Gly466Ala
|
|