ENST00000456935.7:c.2117G>T
MANE Select
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ENSP00000395473.2:p.Gly706Val
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ENST00000221363.8:c.2114G>T
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ENSP00000221363.4:p.Gly705Val
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ENST00000456935.6:c.2117G>T
|
ENSP00000395473.2:p.Gly706Val
|
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ENST00000466794.5:n.2707G>T
|
|
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NM_000528.3:c.2117G>T
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NP_000519.2:p.Gly706Val
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NM_001173498.1:c.2114G>T
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NP_001166969.1:p.Gly705Val
|
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XM_005259913.1:c.2120G>T
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XP_005259970.1:p.Gly707Val
|
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XM_011528017.1:c.1016G>T
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XP_011526319.1:p.Gly339Val
|
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XM_005259913.2:c.2120G>T
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XP_005259970.1:p.Gly707Val
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XM_024451518.1:c.1016G>T
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XP_024307286.1:p.Gly339Val
|
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NM_000528.4:c.2117G>T
MANE Select
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NP_000519.2:p.Gly706Val
|
|
NM_001173498.2:c.2114G>T
|
NP_001166969.1:p.Gly705Val
|
|