ENST00000321612.8:c.1971T>C
MANE Select
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ENSP00000370737.4:p.Ser657=
|
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ENST00000460457.2:n.131T>C
|
|
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ENST00000638233.1:n.406T>C
|
|
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ENST00000638661.1:c.171T>C
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ENSP00000491369.1:p.Ser57=
|
|
ENST00000638694.1:n.158T>C
|
|
|
ENST00000639318.1:c.171T>C
|
ENSP00000491932.1:p.Ser57=
|
|
ENST00000639364.1:n.1671T>C
|
|
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ENST00000639443.1:n.1539T>C
|
|
|
ENST00000639954.1:n.1679T>C
|
|
|
ENST00000640208.1:c.171T>C
|
ENSP00000491895.1:p.Ser57=
|
|
ENST00000640505.1:n.210T>C
|
|
|
ENST00000640592.1:n.1854T>C
|
|
|
ENST00000321612.6:c.1971T>C
|
ENSP00000370737.3:p.Ser657=
|
|
ENST00000460457.1:n.110T>C
|
|
|
NM_000170.2:c.1971T>C , LRG_643t1:c.1971T>C
|
NP_000161.2:p.Ser657=
|
|
NM_000170.3:c.1971T>C
MANE Select
|
NP_000161.2:p.Ser657=
|
|