ENST00000029410.10:c.557C>G
MANE Select
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ENSP00000029410.5:p.Ala186Gly
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ENST00000029410.9:c.557C>G
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ENSP00000029410.5:p.Ala186Gly
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ENST00000502420.1:n.536C>G
|
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ENST00000505145.1:n.1655C>G
|
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ENST00000505433.5:c.*63C>G
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ENSP00000425591.1:n.*63C>G
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ENST00000515353.1:n.81C>G
|
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NM_007255.2:c.557C>G
|
NP_009186.1:p.Ala186Gly
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XM_005265805.2:c.215C>G
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XP_005265862.1:p.Ala72Gly
|
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XM_006714816.2:c.77C>G
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XP_006714879.1:p.Ala26Gly
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XM_011534421.1:c.215C>G
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XP_011532723.1:p.Ala72Gly
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XM_006714816.4:c.77C>G
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XP_006714879.1:p.Ala26Gly
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XM_017008999.2:c.215C>G
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XP_016864488.1:p.Ala72Gly
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NM_007255.3:c.557C>G
MANE Select
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NP_009186.1:p.Ala186Gly
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