ENST00000268125.10:c.566A>C
MANE Select
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ENSP00000268125.5:p.Glu189Ala
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|
ENST00000268125.9:c.566A>C
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ENSP00000268125.5:p.Glu189Ala
|
|
ENST00000567787.1:c.*144A>C
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ENSP00000457251.1:n.*144A>C
|
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NM_000326.4:c.566A>C
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NP_000317.1:p.Glu189Ala
|
|
XM_011521870.1:c.566A>C
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XP_011520172.1:p.Glu189Ala
|
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XM_011521871.1:c.491A>C
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XP_011520173.1:p.Glu164Ala
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XM_011521872.1:c.491A>C
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XP_011520174.1:p.Glu164Ala
|
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XM_011521870.2:c.566A>C
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XP_011520172.1:p.Glu189Ala
|
|
XM_017022460.1:c.593A>C
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XP_016877949.1:p.Glu198Ala
|
|
NM_000326.5:c.566A>C
MANE Select
|
NP_000317.1:p.Glu189Ala
|
|