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NM_006767.4:c.263G>T
MANE Select
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NP_006758.2:p.Gly88Val
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ENST00000646124.2:c.263G>T
MANE Select
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ENSP00000496779.1:p.Gly88Val
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NM_006767.3:c.263G>T
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NP_006758.2:p.Gly88Val
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ENST00000215739.12:c.263G>T
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ENSP00000215739.8:p.Gly88Val
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ENST00000414985.5:c.263G>T
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ENSP00000397247.1:p.Gly88Val
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ENST00000443265.5:c.268G>T
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ENSP00000406466.1:p.Gly90Ter
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ENST00000479606.5:n.409G>T
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ENST00000493460.1:n.338G>T
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ENST00000493460.2:n.338G>T
|
|
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ENST00000642151.1:c.141G>T
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|
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ENST00000644435.1:c.169G>T
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|
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ENST00000645935.1:c.263G>T
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ENSP00000493479.1:p.Gly88Val
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ENST00000700578.1:c.263G>T
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ENSP00000515073.1:p.Gly88Val
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