ENST00000305544.9:c.2885G>T
MANE Select
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ENSP00000307156.4:p.Gly962Val
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ENST00000305544.8:c.2885G>T
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ENSP00000307156.4:p.Gly962Val
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ENST00000418109.5:c.2885G>T
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ENSP00000388325.1:p.Gly962Val
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ENST00000462930.5:n.292G>T
|
|
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ENST00000464891.5:n.618G>T
|
|
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ENST00000483057.1:n.485G>T
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|
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ENST00000542580.1:n.200G>T
|
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NM_002292.3:c.2885G>T
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NP_002283.3:p.Gly962Val
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XM_005265127.3:c.2885G>T
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XP_005265184.1:p.Gly962Val
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XM_005265127.4:c.2885G>T
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XP_005265184.1:p.Gly962Val
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NM_002292.4:c.2885G>T
MANE Select
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NP_002283.3:p.Gly962Val
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