ENST00000266771.10:c.632G>C
MANE Select
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ENSP00000266771.5:p.Gly211Ala
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ENST00000266771.9:c.632G>C
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ENSP00000266771.5:p.Gly211Ala
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ENST00000366292.6:n.944G>C
|
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ENST00000376740.8:c.211G>C
|
|
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ENST00000376744.8:c.468G>C
|
|
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ENST00000535272.1:n.426G>C
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ENST00000539703.1:n.282G>C
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|
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NM_145648.3:c.632G>C
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NP_663623.1:p.Gly211Ala
|
|
XM_011537895.1:c.782G>C
|
XP_011536197.1:p.Gly261Ala
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XR_429081.2:n.655G>C
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XR_944494.1:n.805G>C
|
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XR_944495.1:n.805G>C
|
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XR_944496.1:n.805G>C
|
|
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XR_944497.1:n.805G>C
|
|
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XM_017018791.1:c.782G>C
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XP_016874280.1:p.Gly261Ala
|
|
XM_017018792.1:c.782G>C
|
XP_016874281.1:p.Gly261Ala
|
|
XM_017018793.1:c.632G>C
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XP_016874282.1:p.Gly211Ala
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XR_002957287.1:n.655G>C
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|
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XR_944496.2:n.805G>C
|
|
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NM_145648.4:c.632G>C
MANE Select
|
NP_663623.1:p.Gly211Ala
|
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