ENST00000315491.12:c.1336G=
MANE Select
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ENSP00000320295.7:p.Ala446=
|
|
ENST00000680788.1:n.4757G=
|
|
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ENST00000315491.11:c.1336G=
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ENSP00000320295.7:p.Ala446=
|
|
ENST00000554444.5:c.1120G=
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ENSP00000451617.1:p.Ala374=
|
|
ENST00000555576.5:c.277+2209G=
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ENSP00000452554.1:n.277+2209G=
|
|
ENST00000555609.5:c.*1421G=
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ENSP00000451276.1:n.*1421G=
|
|
ENST00000556922.1:c.2377G=
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ENSP00000451560.1:p.Ala793=
|
|
NM_001197181.1:c.1120G=
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NP_001184110.1:p.Ala374=
|
|
NM_006086.3:c.1336G=
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NP_006077.2:p.Ala446=
|
|
NM_006086.4:c.1336G=
MANE Select
|
NP_006077.2:p.Ala446=
|
|
NM_001197181.2:c.1120G=
|
NP_001184110.1:p.Ala374=
|
|