ENST00000315491.12:c.906C=
MANE Select
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ENSP00000320295.7:p.Ala302=
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|
ENST00000680788.1:n.4327C=
|
|
|
ENST00000315491.11:c.906C=
|
ENSP00000320295.7:p.Ala302=
|
|
ENST00000554444.5:c.690C=
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ENSP00000451617.1:p.Ala230=
|
|
ENST00000555576.5:c.277+1779C=
|
ENSP00000452554.1:n.277+1779C=
|
|
ENST00000555609.5:c.*991C=
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ENSP00000451276.1:n.*991C=
|
|
ENST00000556922.1:c.1947C=
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ENSP00000451560.1:p.Ala649=
|
|
NM_001197181.1:c.690C=
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NP_001184110.1:p.Ala230=
|
|
NM_006086.3:c.906C=
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NP_006077.2:p.Ala302=
|
|
NM_006086.4:c.906C=
MANE Select
|
NP_006077.2:p.Ala302=
|
|
NM_001197181.2:c.690C=
|
NP_001184110.1:p.Ala230=
|
|