ENST00000331373.10:c.528G>T
MANE Select
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ENSP00000331258.5:p.Gln176His
|
|
ENST00000614426.2:c.*324G>T
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ENSP00000478821.2:n.*324G>T
|
|
ENST00000674646.1:c.246G>T
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ENSP00000501703.1:p.Gln82His
|
|
ENST00000674676.1:c.246G>T
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ENSP00000502544.1:p.Gln82His
|
|
ENST00000674782.1:c.*448G>T
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ENSP00000501683.1:n.*448G>T
|
|
ENST00000674937.1:c.486G>T
|
ENSP00000501823.1:p.Gln162His
|
|
ENST00000675322.1:c.246G>T
|
ENSP00000502235.1:p.Gln82His
|
|
ENST00000675675.1:c.246G>T
|
ENSP00000501793.1:p.Gln82His
|
|
ENST00000676178.1:c.*313G>T
|
ENSP00000502007.1:n.*313G>T
|
|
ENST00000676193.1:c.528G>T
|
ENSP00000502774.1:p.Gln176His
|
|
ENST00000331373.9:c.528G>T
|
ENSP00000331258.5:p.Gln176His
|
|
ENST00000614426.1:c.528G>T
|
ENSP00000478821.1:p.Gln176His
|
|
NM_001277971.1:c.528G>T
|
NP_001264900.1:p.Gln176His
|
|
NM_032237.4:c.528G>T
|
NP_115613.1:p.Gln176His
|
|
XM_011544668.1:c.528G>T
|
XP_011542970.1:p.Gln176His
|
|
XM_011544669.1:c.528G>T
|
XP_011542971.1:p.Gln176His
|
|
NM_032237.5:c.528G>T
MANE Select
|
NP_115613.1:p.Gln176His
|
|
NM_001277971.2:c.528G>T
|
NP_001264900.1:p.Gln176His
|
|