ENST00000357578.8:c.566T>G
MANE Select
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ENSP00000350191.3:p.Leu189Arg
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ENST00000672352.1:c.329T>G
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ENSP00000500876.1:p.Leu110Arg
|
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ENST00000672557.1:c.484T>G
|
|
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ENST00000672652.1:c.487T>G
|
|
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ENST00000675422.1:n.1326T>G
|
|
|
ENST00000348925.2:c.566T>G
|
ENSP00000314649.3:p.Leu189Arg
|
|
ENST00000357578.7:c.566T>G
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ENSP00000350191.3:p.Leu189Arg
|
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ENST00000491546.5:c.482T>G
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ENSP00000417687.1:p.Leu161Arg
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NM_001080.3:c.566T>G
MANE Select
|
NP_001071.1:p.Leu189Arg
|
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NM_170740.1:c.566T>G
|
NP_733936.1:p.Leu189Arg
|
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NM_001368954.1:c.566T>G
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NP_001355883.1:p.Leu189Arg
|
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