ENST00000355265.7:c.530G>T
MANE Select
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ENSP00000347409.2:p.Gly177Val
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ENST00000467543.6:c.*382G>T
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ENSP00000420011.2:n.*382G>T
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ENST00000355265.6:c.530G>T
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ENSP00000347409.2:p.Gly177Val
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ENST00000467543.5:c.473G>T
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ENSP00000420011.1:p.Gly158Val
|
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ENST00000476829.5:c.525+335G>T
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ENSP00000419889.1:n.525+335G>T
|
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ENST00000479768.6:n.648G>T
|
|
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ENST00000494148.1:n.129G>T
|
|
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NM_000420.2:c.530G>T
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NP_000411.1:p.Gly177Val
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XM_005249993.2:c.566G>T
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XP_005250050.1:p.Gly189Val
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NM_000420.3:c.530G>T
MANE Select
|
NP_000411.1:p.Gly177Val
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