ENST00000268125.10:c.591C>G
MANE Select
|
ENSP00000268125.5:p.Gly197=
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ENST00000268125.9:c.591C>G
|
ENSP00000268125.5:p.Gly197=
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|
ENST00000563254.1:c.8C>G
|
|
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ENST00000567787.1:c.*169C>G
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ENSP00000457251.1:n.*169C>G
|
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NM_000326.4:c.591C>G
|
NP_000317.1:p.Gly197=
|
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XM_011521870.1:c.591C>G
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XP_011520172.1:p.Gly197=
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XM_011521871.1:c.516C>G
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XP_011520173.1:p.Gly172=
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XM_011521872.1:c.516C>G
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XP_011520174.1:p.Gly172=
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XM_011521870.2:c.591C>G
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XP_011520172.1:p.Gly197=
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XM_017022460.1:c.618C>G
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XP_016877949.1:p.Gly206=
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|
NM_000326.5:c.591C>G
MANE Select
|
NP_000317.1:p.Gly197=
|
|