ENST00000297784.10:c.1855T>G
MANE Select
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ENSP00000297784.6:p.Cys619Gly
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ENST00000644967.1:c.*295T>G
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ENSP00000496159.1:n.*295T>G
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ENST00000645053.1:c.1258-5936T>G
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ENSP00000493838.1:n.1258-5936T>G
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ENST00000645208.2:c.1855T>G
|
ENSP00000494684.1:p.Cys619Gly
|
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ENST00000645773.1:c.1729T>G
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ENSP00000493698.1:p.Cys577Gly
|
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ENST00000645787.1:n.1998T>G
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|
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ENST00000646619.1:c.1417T>G
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ENSP00000493726.1:p.Cys473Gly
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ENST00000651183.1:c.1417T>G
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ENSP00000498723.1:p.Cys473Gly
|
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ENST00000297784.9:c.1855T>G
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ENSP00000297784.5:p.Cys619Gly
|
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ENST00000340019.4:c.1855T>G
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ENSP00000341433.3:p.Cys619Gly
|
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ENST00000469455.1:n.336T>G
|
|
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ENST00000486417.5:n.753T>G
|
|
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NM_138691.2:c.1855T>G
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NP_619636.2:p.Cys619Gly
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XM_011518213.1:c.2443T>G
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XP_011516515.1:p.Cys815Gly
|
|
XM_017014256.1:c.1858T>G
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XP_016869745.1:p.Cys620Gly
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NM_138691.3:c.1855T>G
MANE Select
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NP_619636.2:p.Cys619Gly
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