ENST00000373344.11:c.4455A>C
MANE Select
|
ENSP00000362441.4:p.Lys1485Asn
|
|
ENST00000373344.9:c.4455A>C
|
ENSP00000362441.4:p.Lys1485Asn
|
|
ENST00000395603.7:c.4341A>C
|
ENSP00000378967.3:p.Lys1447Asn
|
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ENST00000480283.5:c.*4083A>C
|
ENSP00000480196.1:n.*4083A>C
|
|
ENST00000623242.3:c.61A>C
|
|
|
NM_000489.4:c.4455A>C
|
NP_000480.3:p.Lys1485Asn
|
|
NM_138270.3:c.4341A>C
|
NP_612114.2:p.Lys1447Asn
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|
XM_005262153.3:c.4452A>C
|
XP_005262210.2:p.Lys1484Asn
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|
XM_005262154.3:c.4368A>C
|
XP_005262211.2:p.Lys1456Asn
|
|
XM_005262155.3:c.4338A>C
|
XP_005262212.2:p.Lys1446Asn
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XM_005262156.3:c.4290A>C
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XP_005262213.2:p.Lys1430Asn
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|
XM_005262157.3:c.4251A>C
|
XP_005262214.2:p.Lys1417Asn
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XM_006724666.2:c.4338A>C
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XP_006724729.1:p.Lys1446Asn
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XM_006724667.2:c.4176A>C
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XP_006724730.1:p.Lys1392Asn
|
|
XM_006724668.2:c.4455A>C
|
XP_006724731.1:p.Lys1485Asn
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|
XR_938400.1:n.4723A>C
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|
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NM_000489.5:c.4455A>C
|
NP_000480.3:p.Lys1485Asn
|
|
XM_005262153.5:c.4452A>C
|
XP_005262210.2:p.Lys1484Asn
|
|
XM_005262154.5:c.4368A>C
|
XP_005262211.2:p.Lys1456Asn
|
|
XM_005262155.4:c.4338A>C
|
XP_005262212.2:p.Lys1446Asn
|
|
XM_005262156.4:c.4290A>C
|
XP_005262213.2:p.Lys1430Asn
|
|
XM_005262157.5:c.4251A>C
|
XP_005262214.2:p.Lys1417Asn
|
|
XM_006724666.4:c.4338A>C
|
XP_006724729.1:p.Lys1446Asn
|
|
XM_006724667.3:c.4176A>C
|
XP_006724730.1:p.Lys1392Asn
|
|
XM_006724668.3:c.4455A>C
|
XP_006724731.1:p.Lys1485Asn
|
|
XM_017029601.2:c.4365A>C
|
XP_016885090.1:p.Lys1455Asn
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|
XM_017029602.1:c.4335A>C
|
XP_016885091.1:p.Lys1445Asn
|
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XM_017029603.1:c.4287A>C
|
XP_016885092.1:p.Lys1429Asn
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XM_017029604.2:c.4254A>C
|
XP_016885093.1:p.Lys1418Asn
|
|
XM_017029605.1:c.4251A>C
|
XP_016885094.1:p.Lys1417Asn
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|
XM_017029606.2:c.4224A>C
|
XP_016885095.1:p.Lys1408Asn
|
|
XM_017029607.2:c.4221A>C
|
XP_016885096.1:p.Lys1407Asn
|
|
XM_017029608.2:c.4173A>C
|
XP_016885097.1:p.Lys1391Asn
|
|
XM_017029609.1:c.4137A>C
|
XP_016885098.1:p.Lys1379Asn
|
|
XM_017029610.1:c.4134A>C
|
XP_016885099.1:p.Lys1378Asn
|
|
XM_017029611.1:c.4089A>C
|
XP_016885100.1:p.Lys1363Asn
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|
XR_001755700.2:n.4680A>C
|
|
|
NM_138270.4:c.4341A>C
|
NP_612114.2:p.Lys1447Asn
|
|
NM_000489.6:c.4455A>C
MANE Select
|
NP_000480.3:p.Lys1485Asn
|
|
NM_138270.5:c.4341A>C
|
NP_612114.2:p.Lys1447Asn
|
|