ENST00000266771.10:c.661A>G
MANE Select
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ENSP00000266771.5:p.Ser221Gly
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ENST00000266771.9:c.661A>G
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ENSP00000266771.5:p.Ser221Gly
|
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ENST00000366292.6:n.973A>G
|
|
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ENST00000376740.8:c.240A>G
|
|
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ENST00000376744.8:c.497A>G
|
|
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ENST00000539703.1:n.311A>G
|
|
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ENST00000614634.1:c.-182A>G
|
ENSP00000483143.1:n.-182A>G
|
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NM_145648.3:c.661A>G
|
NP_663623.1:p.Ser221Gly
|
|
XM_011537895.1:c.811A>G
|
XP_011536197.1:p.Ser271Gly
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XR_429081.2:n.684A>G
|
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XR_944494.1:n.834A>G
|
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XR_944495.1:n.834A>G
|
|
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XR_944496.1:n.834A>G
|
|
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XR_944497.1:n.834A>G
|
|
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XM_017018791.1:c.811A>G
|
XP_016874280.1:p.Ser271Gly
|
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XM_017018792.1:c.811A>G
|
XP_016874281.1:p.Ser271Gly
|
|
XM_017018793.1:c.661A>G
|
XP_016874282.1:p.Ser221Gly
|
|
XR_002957287.1:n.684A>G
|
|
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XR_944496.2:n.834A>G
|
|
|
NM_145648.4:c.661A>G
MANE Select
|
NP_663623.1:p.Ser221Gly
|
|