ENST00000321612.8:c.1998G=
MANE Select
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ENSP00000370737.4:p.Gln666=
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ENST00000460457.2:n.158G=
|
|
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ENST00000638233.1:n.433G=
|
|
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ENST00000638661.1:c.198G=
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ENSP00000491369.1:p.Gln66=
|
|
ENST00000638694.1:n.185G=
|
|
|
ENST00000639318.1:c.198G=
|
ENSP00000491932.1:p.Gln66=
|
|
ENST00000639364.1:n.1698G=
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|
|
ENST00000639443.1:n.1566G=
|
|
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ENST00000639954.1:n.1706G=
|
|
|
ENST00000640208.1:c.198G=
|
ENSP00000491895.1:p.Gln66=
|
|
ENST00000640505.1:n.237G=
|
|
|
ENST00000640592.1:n.1881G=
|
|
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ENST00000321612.6:c.1998G=
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ENSP00000370737.3:p.Gln666=
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|
ENST00000460457.1:n.137G=
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|
|
NM_000170.2:c.1998G= , LRG_643t1:c.1998G=
|
NP_000161.2:p.Gln666=
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|
NM_000170.3:c.1998G=
MANE Select
|
NP_000161.2:p.Gln666=
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|