ENST00000691183.1:c.*163G=
|
ENSP00000509954.1:n.*163G=
|
|
ENST00000378842.8:c.575G=
MANE Select
|
ENSP00000368119.4:p.Ser192=
|
|
ENST00000378842.7:c.575G=
|
ENSP00000368119.3:p.Ser192=
|
|
ENST00000450095.6:c.248G=
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ENSP00000401956.2:p.Ser83=
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|
ENST00000472111.5:n.831G=
|
|
|
ENST00000473506.6:c.*163G=
|
ENSP00000432839.2:n.*163G=
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|
ENST00000473529.5:n.734G=
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|
|
ENST00000485531.1:n.1169G=
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|
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ENST00000487381.5:n.960G=
|
|
|
ENST00000489643.6:n.350G=
|
|
|
ENST00000554085.5:c.*319G=
|
ENSP00000450419.1:n.*319G=
|
|
ENST00000554139.5:n.821G=
|
|
|
ENST00000554550.5:c.*195G=
|
ENSP00000451435.1:n.*195G=
|
|
ENST00000554638.5:n.1047G=
|
|
|
ENST00000554897.5:c.*262G=
|
ENSP00000450942.1:n.*262G=
|
|
ENST00000554944.5:n.924G=
|
|
|
ENST00000555020.5:n.731G=
|
|
|
ENST00000555086.5:n.579G=
|
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|
ENST00000555214.5:n.396G=
|
|
|
ENST00000556244.1:c.562G=
|
|
|
ENST00000556278.1:c.320G=
|
ENSP00000451792.1:p.Ser107=
|
|
ENST00000556494.5:n.696G=
|
|
|
ENST00000557706.5:n.1137G=
|
|
|
NM_000155.3:c.575G=
|
NP_000146.2:p.Ser192=
|
|
NM_001258332.1:c.248G=
|
NP_001245261.1:p.Ser83=
|
|
NM_000155.4:c.575G=
MANE Select
|
NP_000146.2:p.Ser192=
|
|
NM_001258332.2:c.248G=
|
NP_001245261.1:p.Ser83=
|
|