ENST00000480188.2:n.1491G>T
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ENST00000696279.1:c.4777G>T
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ENST00000696280.1:n.4546G>T
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ENST00000696281.1:c.4475G>T
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ENSP00000512521.1:p.Gly1492Val
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ENST00000697921.1:n.3335G>T
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ENST00000697922.1:c.*4447G>T
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ENSP00000513478.1:n.*4447G>T
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ENST00000697923.1:n.4902G>T
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ENST00000223642.3:c.4457G>T
MANE Select
|
ENSP00000223642.1:p.Gly1486Val
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ENST00000223642.2:c.4457G>T
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ENSP00000223642.1:p.Gly1486Val
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NM_001735.2:c.4457G>T , LRG_28t1:c.4457G>T
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NP_001726.2:p.Gly1486Val
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|
XM_011518980.1:c.4472G>T
|
XP_011517282.1:p.Gly1491Val
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NM_001317163.1:c.4475G>T
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NP_001304092.1:p.Gly1492Val
|
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NM_001317163.2:c.4475G>T
|
NP_001304092.1:p.Gly1492Val
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NM_001735.3:c.4457G>T
MANE Select
|
NP_001726.2:p.Gly1486Val
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