ENST00000258385.8:c.317A>G
MANE Select
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ENSP00000258385.3:p.Asp106Gly
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ENST00000258385.7:c.317A>G
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ENSP00000258385.3:p.Asp106Gly
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ENST00000412233.5:c.317A>G
|
ENSP00000398143.1:p.Asp106Gly
|
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ENST00000441621.6:c.317A>G
|
ENSP00000408819.2:p.Asp106Gly
|
|
ENST00000446616.1:c.317A>G
|
ENSP00000410801.1:p.Asp106Gly
|
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ENST00000449596.5:c.272A>G
|
ENSP00000404950.1:p.Asp91Gly
|
|
ENST00000543200.5:c.272A>G
|
ENSP00000438380.1:p.Asp91Gly
|
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NM_000751.2:c.317A>G
|
NP_000742.1:p.Asp106Gly
|
|
NM_001256657.1:c.272A>G
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NP_001243586.1:p.Asp91Gly
|
|
NM_001311195.1:c.46A>G
|
NP_001298124.1:p.Thr16Ala
|
|
NM_001311196.1:c.46A>G
|
NP_001298125.1:p.Thr16Ala
|
|
NR_046333.1:c.-4294966923A>G
|
|
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NR_046334.1:c.-4294966923A>G
|
|
|
XM_011510524.1:c.46A>G
|
XP_011508826.1:p.Thr16Ala
|
|
XM_011510524.2:c.46A>G
|
XP_011508826.1:p.Thr16Ala
|
|
NM_000751.3:c.317A>G
MANE Select
|
NP_000742.1:p.Asp106Gly
|
|
NM_001311195.2:c.46A>G
|
NP_001298124.1:p.Thr16Ala
|
|
NM_001311196.2:c.46A>G
|
NP_001298125.1:p.Thr16Ala
|
|
NM_001256657.2:c.272A>G
|
NP_001243586.1:p.Asp91Gly
|
|