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NM_000170.3:c.1852G>C
MANE Select
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NP_000161.2:p.Gly618Arg
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ENST00000321612.8:c.1852G>C
MANE Select
|
ENSP00000370737.4:p.Gly618Arg
|
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NM_000170.2:c.1852G>C , LRG_643t1:c.1852G>C
|
NP_000161.2:p.Gly618Arg
|
|
ENST00000321612.6:c.1852G>C
|
ENSP00000370737.3:p.Gly618Arg
|
|
ENST00000460457.2:n.12G>C
|
|
|
ENST00000638233.1:n.287G>C
|
|
|
ENST00000638661.1:c.52G>C
|
ENSP00000491369.1:p.Gly18Arg
|
|
ENST00000638694.1:n.39G>C
|
|
|
ENST00000639318.1:c.52G>C
|
ENSP00000491932.1:p.Gly18Arg
|
|
ENST00000639364.1:n.1552G>C
|
|
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ENST00000639443.1:n.1420G>C
|
|
|
ENST00000639954.1:n.1560G>C
|
|
|
ENST00000640208.1:c.52G>C
|
ENSP00000491895.1:p.Gly18Arg
|
|
ENST00000640505.1:n.91G>C
|
|
|
ENST00000640592.1:n.1735G>C
|
|