ENST00000312251.8:c.1157G>T
MANE Select
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ENSP00000310998.3:p.Gly386Val
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ENST00000649828.1:c.*329G>T
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ENSP00000498032.1:n.*329G>T
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ENST00000312251.7:c.1157G>T
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ENSP00000310998.3:p.Gly386Val
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ENST00000381955.7:c.1157G>T
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ENSP00000371381.3:p.Gly386Val
|
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ENST00000562746.5:c.*329G>T
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ENSP00000455900.1:n.*329G>T
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ENST00000563578.5:c.738+1017G>T
|
|
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ENST00000564397.5:n.2210G>T
|
|
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ENST00000565876.5:c.481-484G>T
|
|
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ENST00000566137.5:n.455G>T
|
|
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ENST00000567739.5:n.476G>T
|
|
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ENST00000568202.5:n.1020G>T
|
|
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ENST00000569296.5:c.770G>T
|
ENSP00000465949.1:n.770G>T
|
|
NM_016256.3:c.1157G>T
|
NP_057340.2:p.Gly386Val
|
|
XM_011522517.1:c.1157G>T
|
XP_011520819.1:p.Gly386Val
|
|
XR_243285.1:n.1253G>T
|
|
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XM_011522517.3:c.1157G>T
|
XP_011520819.1:p.Gly386Val
|
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XR_001751908.2:n.1252G>T
|
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XR_001751909.2:n.1256G>T
|
|
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XR_001751910.2:n.1285G>T
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XR_001751911.2:n.1285G>T
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|
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XR_001751912.2:n.1289G>T
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|
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NM_016256.4:c.1157G>T
MANE Select
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NP_057340.2:p.Gly386Val
|
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