ENST00000321612.8:c.1941G=
MANE Select
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ENSP00000370737.4:p.Pro647=
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ENST00000460457.2:n.101G=
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|
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ENST00000638233.1:n.376G=
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|
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ENST00000638661.1:c.141G=
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ENSP00000491369.1:p.Pro47=
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ENST00000638694.1:n.128G=
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|
|
ENST00000639318.1:c.141G=
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ENSP00000491932.1:p.Pro47=
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|
ENST00000639364.1:n.1641G=
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|
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ENST00000639443.1:n.1509G=
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|
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ENST00000639954.1:n.1649G=
|
|
|
ENST00000640208.1:c.141G=
|
ENSP00000491895.1:p.Pro47=
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|
ENST00000640505.1:n.180G=
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|
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ENST00000640592.1:n.1824G=
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|
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ENST00000321612.6:c.1941G=
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ENSP00000370737.3:p.Pro647=
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|
ENST00000460457.1:n.80G=
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|
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NM_000170.2:c.1941G= , LRG_643t1:c.1941G=
|
NP_000161.2:p.Pro647=
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|
NM_000170.3:c.1941G=
MANE Select
|
NP_000161.2:p.Pro647=
|
|