ENST00000269980.7:c.692T>G
MANE Select
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ENSP00000269980.2:p.Val231Gly
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ENST00000269980.6:c.692T>G
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ENSP00000269980.2:p.Val231Gly
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ENST00000457836.6:c.626T>G
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ENSP00000416000.2:p.Val209Gly
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ENST00000535632.5:n.321T>G
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ENST00000540732.3:c.794T>G
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ENSP00000443246.1:p.Val265Gly
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ENST00000541315.1:c.592T>G
|
|
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ENST00000542943.5:c.605T>G
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ENSP00000440345.1:p.Val202Gly
|
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ENST00000545787.1:n.320T>G
|
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ENST00000595085.5:c.692T>G
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ENSP00000471150.2:p.Val231Gly
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NM_000709.3:c.692T>G
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NP_000700.1:p.Val231Gly
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NM_001164783.1:c.692T>G
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NP_001158255.1:p.Val231Gly
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NM_000709.4:c.692T>G
MANE Select
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NP_000700.1:p.Val231Gly
|
|
NM_001164783.2:c.692T>G
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NP_001158255.1:p.Val231Gly
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