ENST00000355943.8:c.1238T>A
MANE Select
|
ENSP00000348211.3:p.Leu413His
|
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ENST00000355943.7:c.1238T>A
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ENSP00000348211.3:p.Leu413His
|
|
ENST00000447245.6:c.995T>A
|
ENSP00000399717.2:p.Leu332His
|
|
ENST00000504098.1:c.800T>A
|
ENSP00000425708.1:p.Leu267His
|
|
ENST00000509432.1:c.599T>A
|
ENSP00000426604.1:p.Leu200His
|
|
ENST00000513706.2:n.2838T>A
|
|
|
ENST00000513807.5:c.752T>A
|
ENSP00000421134.1:p.Leu251His
|
|
NM_001303249.1:c.995T>A
|
NP_001290178.1:p.Leu332His
|
|
NM_001303250.1:c.965T>A
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NP_001290179.1:p.Leu322His
|
|
NM_138773.2:c.1238T>A
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NP_620128.1:p.Leu413His
|
|
NM_001303249.2:c.995T>A
|
NP_001290178.1:p.Leu332His
|
|
NM_001303250.2:c.965T>A
|
NP_001290179.1:p.Leu322His
|
|
NM_138773.3:c.1238T>A
|
NP_620128.1:p.Leu413His
|
|
NR_138151.1:n.1512T>A
|
|
|
NM_138773.4:c.1238T>A
MANE Select
|
NP_620128.1:p.Leu413His
|
|
NM_001303249.3:c.995T>A
|
NP_001290178.1:p.Leu332His
|
|
NM_001303250.3:c.965T>A
|
NP_001290179.1:p.Leu322His
|
|
NR_138151.2:n.1477T>A
|
|
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