ENST00000334785.12:c.1557A>T
MANE Select
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ENSP00000333938.7:p.Gln519His
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ENST00000330010.12:c.1365A>T
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ENSP00000327363.8:p.Gln455His
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|
ENST00000334785.11:c.1557A>T
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ENSP00000333938.7:p.Gln519His
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ENST00000342754.5:c.1256A>T
|
|
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ENST00000470735.1:n.396A>T
|
|
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ENST00000480732.2:n.1131A>T
|
|
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NM_001172309.1:c.1365A>T
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NP_001165780.1:p.Gln455His
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NM_144573.3:c.1557A>T , LRG_442t1:c.1557A>T
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NP_653174.3:p.Gln519His
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XM_005271322.2:c.1557A>T
|
XP_005271379.1:p.Gln519His
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XM_005271323.2:c.1515A>T
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XP_005271380.1:p.Gln505His
|
|
XM_005271324.3:c.1365A>T
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XP_005271381.1:p.Gln455His
|
|
XM_005271325.2:c.1335A>T
|
XP_005271382.1:p.Gln445His
|
|
XM_005271326.2:c.1323A>T
|
XP_005271383.1:p.Gln441His
|
|
XM_005271327.2:c.1140A>T
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XP_005271384.1:p.Gln380His
|
|
XM_005271322.4:c.1557A>T
|
XP_005271379.1:p.Gln519His
|
|
XM_005271323.4:c.1515A>T
|
XP_005271380.1:p.Gln505His
|
|
XM_005271324.5:c.1365A>T
|
XP_005271381.1:p.Gln455His
|
|
XM_005271325.4:c.1335A>T
|
XP_005271382.1:p.Gln445His
|
|
XM_005271326.4:c.1323A>T
|
XP_005271383.1:p.Gln441His
|
|
XM_005271327.4:c.1140A>T
|
XP_005271384.1:p.Gln380His
|
|
NM_001172309.2:c.1365A>T
|
NP_001165780.1:p.Gln455His
|
|
NM_144573.4:c.1557A>T
MANE Select
|
NP_653174.3:p.Gln519His
|
|