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NM_003000.3:c.206G>T
MANE Select
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NP_002991.2:p.Gly69Val
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ENST00000375499.8:c.206G>T
MANE Select
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ENSP00000364649.3:p.Gly69Val
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NM_003000.2:c.206G>T , LRG_316t1:c.206G>T
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NP_002991.2:p.Gly69Val
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ENST00000375499.7:c.206G>T
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ENSP00000364649.3:p.Gly69Val
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ENST00000463045.2:c.35G>T
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ENSP00000481376.1:p.Gly12Val
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ENST00000463045.3:c.35G>T
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ENSP00000481376.2:p.Gly12Val
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ENST00000466613.2:n.218G>T
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|
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ENST00000475506.1:n.123G>T
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|
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ENST00000485515.5:n.194G>T
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|
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ENST00000491274.5:c.164G>T
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ENSP00000480482.1:p.Gly55Val
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ENST00000491274.6:c.164G>T
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ENSP00000480482.2:p.Gly55Val
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