ENST00000682422.1:n.905G=
|
|
|
ENST00000682545.1:c.*330G=
|
ENSP00000508402.1:n.*330G=
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|
ENST00000682887.1:c.1725G=
|
ENSP00000506946.1:n.1725G=
|
|
ENST00000683302.1:c.1255G=
|
ENSP00000507885.1:p.Ala419=
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|
ENST00000683557.1:c.*156G=
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ENSP00000508029.1:n.*156G=
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|
ENST00000367282.6:c.1324G=
MANE Select
|
ENSP00000356251.4:p.Ala442=
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|
ENST00000367282.5:c.1324G=
|
ENSP00000356251.4:p.Ala442=
|
|
NM_004767.3:c.1324G=
|
NP_004758.3:p.Ala442=
|
|
XM_011510158.1:c.763G=
|
XP_011508460.1:p.Ala255=
|
|
NM_004767.4:c.1324G=
|
NP_004758.3:p.Ala442=
|
|
XM_011510158.2:c.763G=
|
XP_011508460.1:p.Ala255=
|
|
NM_004767.5:c.1324G=
MANE Select
|
NP_004758.3:p.Ala442=
|
|