ENST00000342245.9:c.1299T=
MANE Select
|
ENSP00000340409.4:p.Cys433=
|
|
ENST00000342245.8:c.1299T=
|
ENSP00000340409.4:p.Cys433=
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|
ENST00000526280.1:c.356T=
|
|
|
ENST00000527275.5:c.1296T=
|
ENSP00000435350.1:p.Cys432=
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|
ENST00000531303.5:c.*130T=
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ENSP00000432625.1:n.*130T=
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|
ENST00000531336.1:n.131T=
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|
|
ENST00000532367.1:n.135T=
|
|
|
ENST00000533123.5:c.*26T=
|
ENSP00000435950.1:n.*26T=
|
|
ENST00000534405.5:c.*130T=
|
ENSP00000434353.1:n.*130T=
|
|
NM_000543.4:c.1299T=
|
NP_000534.3:p.Cys433=
|
|
NM_001007593.2:c.1296T=
|
NP_001007594.2:p.Cys432=
|
|
XM_005253075.3:c.1299T=
|
XP_005253132.1:p.Cys433=
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|
XM_011520303.1:c.1167T=
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XP_011518605.1:p.Cys389=
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|
XM_011520304.1:c.1167T=
|
XP_011518606.1:p.Cys389=
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|
XR_930886.1:n.1637T=
|
|
|
NM_001318087.1:c.1299T=
|
NP_001305016.1:p.Cys433=
|
|
NM_001318088.1:c.378T=
|
NP_001305017.1:p.Cys126=
|
|
NM_001365135.1:c.1167T=
|
NP_001352064.1:p.Cys389=
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|
NR_027400.2:n.1312T=
|
|
|
NR_134502.1:n.831T=
|
|
|
XM_011520304.2:c.1167T=
|
XP_011518606.1:p.Cys389=
|
|
XR_001747940.2:n.1464T=
|
|
|
XR_002957158.1:n.1464T=
|
|
|
NM_000543.5:c.1299T=
MANE Select
|
NP_000534.3:p.Cys433=
|
|
NM_001007593.3:c.1296T=
|
NP_001007594.2:p.Cys432=
|
|
NM_001318087.2:c.1299T=
|
NP_001305016.1:p.Cys433=
|
|
NM_001318088.2:c.378T=
|
NP_001305017.1:p.Cys126=
|
|
NM_001365135.2:c.1167T=
|
NP_001352064.1:p.Cys389=
|
|
NR_027400.3:n.1252T=
|
|
|
NR_134502.2:n.771T=
|
|
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