ENST00000433363.7:c.956T>G
MANE Select
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ENSP00000406220.2:p.Val319Gly
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ENST00000293800.10:c.905T>G
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ENSP00000293800.6:p.Val302Gly
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ENST00000381074.8:c.827T>G
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ENSP00000370464.4:p.Val276Gly
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ENST00000433363.6:c.956T>G
|
ENSP00000406220.2:p.Val319Gly
|
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ENST00000572094.1:c.*706T>G
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ENSP00000461495.1:n.*706T>G
|
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ENST00000572727.1:n.65T>G
|
|
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ENST00000573648.5:c.956T>G
|
ENSP00000459372.1:p.Val319Gly
|
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ENST00000574824.5:n.2089T>G
|
|
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NM_001143838.2:c.956T>G
|
NP_001137310.1:p.Val319Gly
|
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NM_001284509.1:c.905T>G
|
NP_001271438.1:p.Val302Gly
|
|
NM_001284510.1:c.827T>G
|
NP_001271439.1:p.Val276Gly
|
|
NM_177550.4:c.956T>G , LRG_1020t1:c.956T>G
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NP_808218.1:p.Val319Gly
|
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XM_006721504.2:c.845T>G
|
XP_006721567.1:p.Val282Gly
|
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XM_011523795.1:c.956T>G
|
XP_011522097.1:p.Val319Gly
|
|
XM_011523795.3:c.956T>G
|
XP_011522097.1:p.Val319Gly
|
|
NM_001143838.3:c.956T>G
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NP_001137310.1:p.Val319Gly
|
|
NM_001284509.2:c.905T>G
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NP_001271438.1:p.Val302Gly
|
|
NM_001284510.2:c.827T>G
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NP_001271439.1:p.Val276Gly
|
|
NM_177550.5:c.956T>G
MANE Select
|
NP_808218.1:p.Val319Gly
|
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