ENST00000053867.8:c.1375A>G
MANE Select
|
ENSP00000053867.2:p.Ser459Gly
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ENST00000639447.1:c.1137-319A>G
|
ENSP00000492014.1:n.1137-319A>G
|
|
ENST00000053867.7:c.1375A>G
|
ENSP00000053867.2:p.Ser459Gly
|
|
ENST00000586242.1:c.9A>G
|
|
|
ENST00000586443.1:c.816A>G
|
|
|
ENST00000589265.5:c.904A>G
|
ENSP00000467616.1:p.Ser302Gly
|
|
NM_002087.3:c.1375A>G
|
NP_002078.1:p.Ser459Gly
|
|
XM_005257253.1:c.1375A>G
|
XP_005257310.1:p.Ser459Gly
|
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XM_024450730.1:c.1375A>G
|
XP_024306498.1:p.Ser459Gly
|
|
NM_002087.4:c.1375A>G
MANE Select
|
NP_002078.1:p.Ser459Gly
|
|