ENST00000268125.10:c.590G>T
MANE Select
|
ENSP00000268125.5:p.Gly197Val
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ENST00000268125.9:c.590G>T
|
ENSP00000268125.5:p.Gly197Val
|
|
ENST00000563254.1:c.7G>T
|
|
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ENST00000567787.1:c.*168G>T
|
ENSP00000457251.1:n.*168G>T
|
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NM_000326.4:c.590G>T
|
NP_000317.1:p.Gly197Val
|
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XM_011521870.1:c.590G>T
|
XP_011520172.1:p.Gly197Val
|
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XM_011521871.1:c.515G>T
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XP_011520173.1:p.Gly172Val
|
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XM_011521872.1:c.515G>T
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XP_011520174.1:p.Gly172Val
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XM_011521870.2:c.590G>T
|
XP_011520172.1:p.Gly197Val
|
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XM_017022460.1:c.617G>T
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XP_016877949.1:p.Gly206Val
|
|
NM_000326.5:c.590G>T
MANE Select
|
NP_000317.1:p.Gly197Val
|
|