ENST00000369538.4:c.417A>C
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ENSP00000358551.4:p.Ala139=
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ENST00000520113.7:c.429A>C
MANE Select
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ENSP00000430075.3:p.Ala143=
|
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ENST00000637080.1:c.432A>C
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ENSP00000489753.1:p.Ala144=
|
|
ENST00000639077.1:n.94A>C
|
|
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ENST00000369538.3:c.516A>C
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ENSP00000358551.3:p.Ala172=
|
|
ENST00000485564.3:n.303A>C
|
|
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ENST00000520113.6:c.528A>C
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ENSP00000430075.2:p.Ala176=
|
|
NM_000036.2:c.528A>C
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NP_000027.2:p.Ala176=
|
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NM_001172626.1:c.516A>C
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NP_001166097.1:p.Ala172=
|
|
NM_000036.3:c.429A>C
MANE Select
|
NP_000027.3:p.Ala143=
|
|
NM_001172626.2:c.417A>C
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NP_001166097.2:p.Ala139=
|
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