ENST00000285398.7:c.454A>G
MANE Select
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ENSP00000285398.2:p.Ile152Val
|
|
ENST00000642308.1:c.454A>G
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ENSP00000496684.1:p.Ile152Val
|
|
ENST00000644317.1:c.312A>G
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ENSP00000494012.1:p.Glu104=
|
|
ENST00000645233.1:c.454A>G
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ENSP00000494116.1:p.Ile152Val
|
|
ENST00000645467.1:c.454A>G
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ENSP00000494889.1:p.Ile152Val
|
|
ENST00000645736.1:c.310A>G
|
ENSP00000494545.1:p.Ile104Val
|
|
ENST00000646654.1:c.454A>G
|
ENSP00000494526.1:p.Ile152Val
|
|
ENST00000647169.1:c.454A>G
|
ENSP00000495619.1:p.Ile152Val
|
|
ENST00000647496.1:c.27A>G
|
|
|
ENST00000285398.6:c.454A>G
|
ENSP00000285398.2:p.Ile152Val
|
|
ENST00000426778.5:c.*435A>G
|
ENSP00000415335.1:n.*435A>G
|
|
ENST00000445889.5:c.*497A>G
|
ENSP00000390888.1:n.*497A>G
|
|
ENST00000462306.5:n.368A>G
|
|
|
ENST00000490062.1:n.384A>G
|
|
|
ENST00000494464.5:n.338A>G
|
|
|
NM_000122.1:c.454A>G , LRG_462t1:c.454A>G
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NP_000113.1:p.Ile152Val
|
|
NM_001303416.1:c.262A>G
|
NP_001290345.1:p.Ile88Val
|
|
NM_001303418.1:c.262A>G
|
NP_001290347.1:p.Ile88Val
|
|
XM_011510794.1:c.454A>G
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XP_011509096.1:p.Ile152Val
|
|
XM_011510795.1:c.-3A>G
|
XP_011509097.1:n.-3A>G
|
|
XM_011510794.2:c.454A>G
|
XP_011509096.1:p.Ile152Val
|
|
XM_017003583.1:c.-3A>G
|
XP_016859072.1:n.-3A>G
|
|
NM_000122.2:c.454A>G
MANE Select
|
NP_000113.1:p.Ile152Val
|
|
NM_001303416.2:c.262A>G
|
NP_001290345.1:p.Ile88Val
|
|
NM_001303418.2:c.262A>G
|
NP_001290347.1:p.Ile88Val
|
|