ENST00000253122.10:c.1358T>A
MANE Select
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ENSP00000253122.5:p.Leu453His
|
|
ENST00000253122.9:c.1358T>A
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ENSP00000253122.5:p.Leu453His
|
|
ENST00000413787.1:c.287T>A
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ENSP00000400463.1:p.Leu96His
|
|
ENST00000430077.6:c.1013T>A
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ENSP00000403041.2:p.Leu338His
|
|
ENST00000442457.1:c.412T>A
|
|
|
ENST00000485324.1:n.1503T>A
|
|
|
NM_001142805.1:c.1328T>A
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NP_001136277.1:p.Leu443His
|
|
NM_001142806.1:c.1013T>A
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NP_001136278.1:p.Leu338His
|
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NM_005629.3:c.1358T>A
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NP_005620.1:p.Leu453His
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NM_005629.4:c.1358T>A
MANE Select
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NP_005620.1:p.Leu453His
|
|
NM_001142805.2:c.1328T>A
|
NP_001136277.1:p.Leu443His
|
|