ENST00000700061.1:c.1081C>G
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ENST00000700062.1:c.1081C>G
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ENST00000700065.1:n.2997C>G
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ENST00000281513.10:c.2984C>G
MANE Select
|
ENSP00000281513.5:p.Ala995Gly
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ENST00000281513.9:c.2984C>G
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ENSP00000281513.5:p.Ala995Gly
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ENST00000429842.1:c.276C>G
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ENST00000441755.5:c.125C>G
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ENSP00000396501.1:p.Ala42Gly
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ENST00000442506.5:c.127C>G
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NM_015909.3:c.2984C>G
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NP_056993.2:p.Ala995Gly
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NR_052013.2:n.3028C>G
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XM_011510357.1:c.2855C>G
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XP_011508659.1:p.Ala952Gly
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XM_011510358.1:c.2984C>G
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XP_011508660.1:p.Ala995Gly
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XM_011510359.1:c.2345C>G
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XP_011508661.1:p.Ala782Gly
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XM_011510360.1:c.785C>G
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XP_011508662.1:p.Ala262Gly
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XM_011510361.1:c.776C>G
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XP_011508663.1:p.Ala259Gly
|
|
XM_011510357.2:c.2855C>G
|
XP_011508659.1:p.Ala952Gly
|
|
XM_011510358.2:c.2984C>G
|
XP_011508660.1:p.Ala995Gly
|
|
XM_011510360.2:c.785C>G
|
XP_011508662.1:p.Ala262Gly
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|
XM_011510361.2:c.776C>G
|
XP_011508663.1:p.Ala259Gly
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|
XM_017004317.1:c.2984C>G
|
XP_016859806.1:p.Ala995Gly
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|
XM_024452961.1:c.2345C>G
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XP_024308729.1:p.Ala782Gly
|
|
NM_015909.4:c.2984C>G
MANE Select
|
NP_056993.2:p.Ala995Gly
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NR_052013.3:n.3014C>G
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