ENST00000369244.7:c.1786T>G
MANE Select
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ENSP00000358247.1:p.Ser596Ala
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ENST00000229971.2:c.1786T>G
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ENSP00000229971.1:p.Ser596Ala
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ENST00000369244.6:c.1786T>G
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ENSP00000358247.1:p.Ser596Ala
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NM_001278716.1:c.1786T>G
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NP_001265645.1:p.Ser596Ala
|
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NM_012160.4:c.1786T>G
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NP_036292.2:p.Ser596Ala
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NR_103836.1:n.1831T>G
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|
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XM_005266930.1:c.1714T>G
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XP_005266987.1:p.Ser572Ala
|
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XM_005266930.3:c.1714T>G
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XP_005266987.1:p.Ser572Ala
|
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XM_017010726.1:c.1786T>G
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XP_016866215.1:p.Ser596Ala
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XM_017010727.2:c.1714T>G
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XP_016866216.1:p.Ser572Ala
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XM_017010728.1:c.1060T>G
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XP_016866217.1:p.Ser354Ala
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|
NM_001278716.2:c.1786T>G
MANE Select
|
NP_001265645.1:p.Ser596Ala
|
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NR_103836.2:n.1771T>G
|
|
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NM_012160.5:c.1786T>G
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NP_036292.2:p.Ser596Ala
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