NM_153000.5:c.754C>G
MANE Select
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NP_694545.1:p.Pro252Ala
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ENST00000355285.10:c.754C>G
MANE Select
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ENSP00000347433.4:p.Pro252Ala
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NM_153000.4:c.754C>G
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NP_694545.1:p.Pro252Ala
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ENST00000355285.9:c.754C>G
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ENSP00000347433.4:p.Pro252Ala
|
ENST00000423585.2:c.59-13421C>G
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ENSP00000404930.2:n.59-13421C>G
|
ENST00000578882.1:c.453+301C>G
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ENSP00000463104.1:n.453+301C>G
|
ENST00000579685.1:c.35C>G
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ENSP00000464649.1:p.Ala12Gly
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ENST00000582723.1:c.*501C>G
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ENSP00000463110.1:n.*501C>G
|
ENST00000584596.2:c.206C>G
|
|
XM_011525603.1:c.754C>G
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XP_011523905.1:p.Pro252Ala
|
XM_011525603.2:c.754C>G
|
XP_011523905.1:p.Pro252Ala
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