ENST00000258385.8:c.1132A>G
MANE Select
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ENSP00000258385.3:p.Ser378Gly
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ENST00000258385.7:c.1132A>G
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ENSP00000258385.3:p.Ser378Gly
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ENST00000441621.6:c.*314A>G
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ENSP00000408819.2:n.*314A>G
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ENST00000446616.1:c.*773A>G
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ENSP00000410801.1:n.*773A>G
|
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ENST00000543200.5:c.1087A>G
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ENSP00000438380.1:p.Ser363Gly
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NM_000751.2:c.1132A>G
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NP_000742.1:p.Ser378Gly
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NM_001256657.1:c.1087A>G
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NP_001243586.1:p.Ser363Gly
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NM_001311195.1:c.550A>G
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NP_001298124.1:p.Ser184Gly
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NM_001311196.1:c.829A>G
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NP_001298125.1:p.Ser277Gly
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NR_046333.1:c.-4294966419A>G
|
|
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NR_046334.1:c.-4294966140A>G
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|
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XM_011510524.1:c.751A>G
|
XP_011508826.1:p.Ser251Gly
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XM_011510524.2:c.751A>G
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XP_011508826.1:p.Ser251Gly
|
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NM_000751.3:c.1132A>G
MANE Select
|
NP_000742.1:p.Ser378Gly
|
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NM_001311195.2:c.550A>G
|
NP_001298124.1:p.Ser184Gly
|
|
NM_001311196.2:c.829A>G
|
NP_001298125.1:p.Ser277Gly
|
|
NM_001256657.2:c.1087A>G
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NP_001243586.1:p.Ser363Gly
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