ENST00000534624.6:c.1566T>C
MANE Select
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ENSP00000432083.1:p.Ala522=
|
|
ENST00000227378.7:c.1566T>C
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ENSP00000227378.3:p.Ala522=
|
|
ENST00000453788.6:c.1387+326T>C
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ENSP00000404372.2:n.1387+326T>C
|
|
ENST00000524552.5:c.339T>C
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ENSP00000435908.1:p.Ala113=
|
|
ENST00000526110.5:c.1509T>C
|
ENSP00000433584.1:p.Ala503=
|
|
ENST00000526686.1:c.222T>C
|
ENSP00000435019.1:p.Ala74=
|
|
ENST00000532091.1:n.1688T>C
|
|
|
ENST00000532636.5:c.1566T>C
|
ENSP00000437125.1:p.Ala522=
|
|
ENST00000533540.5:c.1128T>C
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ENSP00000437189.1:p.Ala376=
|
|
ENST00000534319.5:c.858T>C
|
ENSP00000433316.1:p.Ala286=
|
|
ENST00000534624.5:c.1566T>C
|
ENSP00000432083.1:p.Ala522=
|
|
NM_006597.5:c.1566T>C
|
NP_006588.1:p.Ala522=
|
|
NM_153201.3:c.1387+326T>C
|
NP_694881.1:n.1387+326T>C
|
|
XM_011542798.1:c.1566T>C
|
XP_011541100.1:p.Ala522=
|
|
NM_006597.6:c.1566T>C
MANE Select
|
NP_006588.1:p.Ala522=
|
|
NM_153201.4:c.1387+326T>C
|
NP_694881.1:n.1387+326T>C
|
|