ENST00000344209.10:c.1493G>T
MANE Select
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ENSP00000345667.5:p.Gly498Val
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ENST00000460554.2:n.1443G>T
|
|
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ENST00000642615.1:c.*676G>T
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ENSP00000495499.1:n.*676G>T
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ENST00000273691.7:c.1361G>T
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ENSP00000273691.3:p.Gly454Val
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ENST00000344209.9:c.1493G>T
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ENSP00000345667.5:p.Gly498Val
|
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ENST00000393631.5:c.1226G>T
|
ENSP00000377251.1:p.Gly409Val
|
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ENST00000460554.1:n.1595G>T
|
|
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ENST00000462014.1:c.1397G>T
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ENSP00000419414.1:p.Gly466Val
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NM_001199799.1:c.1493G>T
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NP_001186728.1:p.Gly498Val
|
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NM_001199800.1:c.1226G>T
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NP_001186729.1:p.Gly409Val
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NM_175924.3:c.1361G>T
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NP_787120.1:p.Gly454Val
|
|
XM_005247389.3:c.1397G>T
|
XP_005247446.1:p.Gly466Val
|
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XM_011512738.1:c.1493G>T
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XP_011511040.1:p.Gly498Val
|
|
XM_011512739.1:c.956G>T
|
XP_011511041.1:p.Gly319Val
|
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XM_005247389.4:c.1397G>T
|
XP_005247446.1:p.Gly466Val
|
|
XM_011512738.2:c.1493G>T
|
XP_011511040.1:p.Gly498Val
|
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XM_011512739.2:c.956G>T
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XP_011511041.1:p.Gly319Val
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NM_001199799.2:c.1493G>T
MANE Select
|
NP_001186728.1:p.Gly498Val
|
|
NM_001199800.2:c.1226G>T
|
NP_001186729.1:p.Gly409Val
|
|
NM_175924.4:c.1361G>T
|
NP_787120.1:p.Gly454Val
|
|