ENST00000264381.8:c.1266G>C
MANE Select
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ENSP00000264381.3:p.Gly422=
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ENST00000264381.7:c.1266G>C
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ENSP00000264381.3:p.Gly422=
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ENST00000479451.5:c.107+7546G>C
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ENSP00000418325.1:n.107+7546G>C
|
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ENST00000482958.1:c.1266G>C
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ENSP00000419804.1:p.Gly422=
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ENST00000488954.1:c.107+7546G>C
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ENSP00000418504.1:n.107+7546G>C
|
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ENST00000497011.5:c.1266G>C
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ENSP00000419505.1:p.Gly422=
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NM_000055.2:c.1266G>C
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NP_000046.1:p.Gly422=
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XM_005247685.1:c.1389G>C
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XP_005247742.1:p.Gly463=
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NM_000055.3:c.1266G>C
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NP_000046.1:p.Gly422=
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NR_137635.1:n.159+7546G>C
|
|
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NR_137636.1:n.1433G>C
|
|
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NM_000055.4:c.1266G>C
MANE Select
|
NP_000046.1:p.Gly422=
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NR_137635.2:n.110+7546G>C
|
|
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NR_137636.2:n.1384G>C
|
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