ENST00000461280.2:n.1199C>A
|
|
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ENST00000683359.1:n.25C>A
|
|
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ENST00000684241.1:n.2734C>A
|
|
|
ENST00000262186.10:c.1901C>A
MANE Select
|
ENSP00000262186.5:p.Thr634Asn
|
|
ENST00000330883.9:c.881C>A
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ENSP00000328531.4:p.Thr294Asn
|
|
ENST00000262186.9:c.1901C>A
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ENSP00000262186.5:p.Thr634Asn
|
|
ENST00000330883.8:c.881C>A
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ENSP00000328531.4:p.Thr294Asn
|
|
ENST00000430723.4:c.1553C>A
|
ENSP00000387657.4:p.Thr518Asn
|
|
ENST00000461280.1:n.1188C>A
|
|
|
ENST00000473610.5:n.1206C>A
|
|
|
ENST00000532957.5:n.2124C>A
|
|
|
NM_000238.3:c.1901C>A , LRG_288t1:c.1901C>A
|
NP_000229.1:p.Thr634Asn
|
|
NM_001204798.1:c.881C>A
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NP_001191727.1:p.Thr294Asn
|
|
NM_172056.2:c.1901C>A , LRG_288t2:c.1901C>A
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NP_742053.1:p.Thr634Asn
|
|
NM_172057.2:c.881C>A , LRG_288t3:c.881C>A
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NP_742054.1:p.Thr294Asn
|
|
XM_011516185.1:c.1601C>A
|
XP_011514487.1:p.Thr534Asn
|
|
XM_011516186.1:c.1901C>A
|
XP_011514488.1:p.Thr634Asn
|
|
XM_011516185.2:c.1601C>A
|
XP_011514487.1:p.Thr534Asn
|
|
XM_011516186.3:c.1901C>A
|
XP_011514488.1:p.Thr634Asn
|
|
XM_017012195.1:c.1751C>A
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XP_016867684.1:p.Thr584Asn
|
|
XM_017012196.1:c.1724C>A
|
XP_016867685.1:p.Thr575Asn
|
|
NM_000238.4:c.1901C>A
MANE Select
|
NP_000229.1:p.Thr634Asn
|
|
NM_001204798.2:c.881C>A
|
NP_001191727.1:p.Thr294Asn
|
|
NM_172057.3:c.881C>A
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NP_742054.1:p.Thr294Asn
|
|