ENST00000267163.6:c.2651A>C
MANE Select
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ENSP00000267163.4:p.Glu884Ala
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ENST00000643064.1:c.194+95388A>C
|
|
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ENST00000650461.1:c.2651A>C
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ENSP00000497193.1:p.Glu884Ala
|
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ENST00000267163.4:c.2651A>C
|
ENSP00000267163.4:p.Glu884Ala
|
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ENST00000484879.1:n.385A>C
|
|
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ENST00000531171.5:n.254A>C
|
|
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NM_000321.2:c.2651A>C , LRG_517t1:c.2651A>C
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NP_000312.2:p.Glu884Ala
|
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XM_011535171.1:c.2390A>C
|
XP_011533473.1:p.Glu797Ala
|
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XM_011535171.2:c.2390A>C
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XP_011533473.1:p.Glu797Ala
|
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NM_000321.3:c.2651A>C
MANE Select
|
NP_000312.2:p.Glu884Ala
|
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