ENST00000553106.6:c.1265A>C
MANE Select
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ENSP00000448059.1:p.Glu422Ala
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ENST00000307000.7:c.1250A>C
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ENSP00000303500.2:p.Glu417Ala
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ENST00000551114.2:n.927A>C
|
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ENST00000553106.5:c.1265A>C
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ENSP00000448059.1:p.Glu422Ala
|
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ENST00000635477.1:c.369A>C
|
|
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ENST00000635528.1:n.780A>C
|
|
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NM_000277.1:c.1265A>C
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NP_000268.1:p.Glu422Ala
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XM_011538422.1:c.1208A>C
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XP_011536724.1:p.Glu403Ala
|
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NM_000277.2:c.1265A>C
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NP_000268.1:p.Glu422Ala
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NM_001354304.1:c.1265A>C
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NP_001341233.1:p.Glu422Ala
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NM_000277.3:c.1265A>C
MANE Select
|
NP_000268.1:p.Glu422Ala
|
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NM_001354304.2:c.1265A>C
|
NP_001341233.1:p.Glu422Ala
|
|