ENST00000700061.1:c.580A>C
|
|
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ENST00000700062.1:c.580A>C
|
|
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ENST00000700065.1:n.2496A>C
|
|
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ENST00000700066.1:c.2000A>C
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ENSP00000514780.1:p.Glu667Ala
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|
ENST00000281513.10:c.2483A>C
MANE Select
|
ENSP00000281513.5:p.Glu828Ala
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ENST00000281513.9:c.2483A>C
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ENSP00000281513.5:p.Glu828Ala
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|
NM_015909.3:c.2483A>C
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NP_056993.2:p.Glu828Ala
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NR_052013.2:n.2527A>C
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|
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XM_011510357.1:c.2354A>C
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XP_011508659.1:p.Glu785Ala
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|
XM_011510358.1:c.2483A>C
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XP_011508660.1:p.Glu828Ala
|
|
XM_011510359.1:c.1844A>C
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XP_011508661.1:p.Glu615Ala
|
|
XM_011510360.1:c.284A>C
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XP_011508662.1:p.Glu95Ala
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|
XM_011510361.1:c.275A>C
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XP_011508663.1:p.Glu92Ala
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|
XM_011510357.2:c.2354A>C
|
XP_011508659.1:p.Glu785Ala
|
|
XM_011510358.2:c.2483A>C
|
XP_011508660.1:p.Glu828Ala
|
|
XM_011510360.2:c.284A>C
|
XP_011508662.1:p.Glu95Ala
|
|
XM_011510361.2:c.275A>C
|
XP_011508663.1:p.Glu92Ala
|
|
XM_017004317.1:c.2483A>C
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XP_016859806.1:p.Glu828Ala
|
|
XM_024452961.1:c.1844A>C
|
XP_024308729.1:p.Glu615Ala
|
|
NM_015909.4:c.2483A>C
MANE Select
|
NP_056993.2:p.Glu828Ala
|
|
NR_052013.3:n.2513A>C
|
|
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