ENST00000216373.10:c.368A>C
MANE Select
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ENSP00000216373.5:p.Asp123Ala
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ENST00000216373.9:c.368A>C
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ENSP00000216373.5:p.Asp123Ala
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ENST00000543680.5:c.368A>C
|
ENSP00000445328.1:p.Asp123Ala
|
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ENST00000555666.1:n.547A>C
|
|
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ENST00000556469.5:n.339A>C
|
|
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NM_006939.2:c.368A>C
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NP_008870.2:p.Asp123Ala
|
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XM_005268021.1:c.188A>C
|
XP_005268078.1:p.Asp63Ala
|
|
XM_011537103.1:c.329A>C
|
XP_011535405.1:p.Asp110Ala
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XM_011537104.1:c.368A>C
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XP_011535406.1:p.Asp123Ala
|
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XR_943842.1:n.1039+15961T>G
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|
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XR_943843.1:n.1039+15961T>G
|
|
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NM_006939.3:c.368A>C
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NP_008870.2:p.Asp123Ala
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NM_006939.4:c.368A>C
MANE Select
|
NP_008870.2:p.Asp123Ala
|
|