ENST00000264381.8:c.1684G>C
MANE Select
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ENSP00000264381.3:p.Gly562Arg
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ENST00000264381.7:c.1684G>C
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ENSP00000264381.3:p.Gly562Arg
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ENST00000479451.5:c.274G>C
|
ENSP00000418325.1:p.Gly92Arg
|
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ENST00000482958.1:c.*190G>C
|
ENSP00000419804.1:n.*190G>C
|
|
ENST00000488954.1:c.274G>C
|
ENSP00000418504.1:p.Glu92Gln
|
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ENST00000497011.5:c.1684G>C
|
ENSP00000419505.1:p.Gly562Arg
|
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NM_000055.2:c.1684G>C
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NP_000046.1:p.Gly562Arg
|
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XM_005247685.1:c.1807G>C
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XP_005247742.1:p.Gly603Arg
|
|
NM_000055.3:c.1684G>C
|
NP_000046.1:p.Gly562Arg
|
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NR_137635.1:n.326G>C
|
|
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NR_137636.1:n.1851G>C
|
|
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NM_000055.4:c.1684G>C
MANE Select
|
NP_000046.1:p.Gly562Arg
|
|
NR_137635.2:n.277G>C
|
|
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NR_137636.2:n.1802G>C
|
|
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