ENST00000373344.11:c.4470A>T
MANE Select
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ENSP00000362441.4:p.Arg1490Ser
|
|
ENST00000373344.9:c.4470A>T
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ENSP00000362441.4:p.Arg1490Ser
|
|
ENST00000395603.7:c.4356A>T
|
ENSP00000378967.3:p.Arg1452Ser
|
|
ENST00000480283.5:c.*4098A>T
|
ENSP00000480196.1:n.*4098A>T
|
|
ENST00000623242.3:c.76A>T
|
|
|
NM_000489.4:c.4470A>T
|
NP_000480.3:p.Arg1490Ser
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|
NM_138270.3:c.4356A>T
|
NP_612114.2:p.Arg1452Ser
|
|
XM_005262153.3:c.4467A>T
|
XP_005262210.2:p.Arg1489Ser
|
|
XM_005262154.3:c.4383A>T
|
XP_005262211.2:p.Arg1461Ser
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|
XM_005262155.3:c.4353A>T
|
XP_005262212.2:p.Arg1451Ser
|
|
XM_005262156.3:c.4305A>T
|
XP_005262213.2:p.Arg1435Ser
|
|
XM_005262157.3:c.4266A>T
|
XP_005262214.2:p.Arg1422Ser
|
|
XM_006724666.2:c.4353A>T
|
XP_006724729.1:p.Arg1451Ser
|
|
XM_006724667.2:c.4191A>T
|
XP_006724730.1:p.Arg1397Ser
|
|
XM_006724668.2:c.4470A>T
|
XP_006724731.1:p.Arg1490Ser
|
|
XR_938400.1:n.4738A>T
|
|
|
NM_000489.5:c.4470A>T
|
NP_000480.3:p.Arg1490Ser
|
|
XM_005262153.5:c.4467A>T
|
XP_005262210.2:p.Arg1489Ser
|
|
XM_005262154.5:c.4383A>T
|
XP_005262211.2:p.Arg1461Ser
|
|
XM_005262155.4:c.4353A>T
|
XP_005262212.2:p.Arg1451Ser
|
|
XM_005262156.4:c.4305A>T
|
XP_005262213.2:p.Arg1435Ser
|
|
XM_005262157.5:c.4266A>T
|
XP_005262214.2:p.Arg1422Ser
|
|
XM_006724666.4:c.4353A>T
|
XP_006724729.1:p.Arg1451Ser
|
|
XM_006724667.3:c.4191A>T
|
XP_006724730.1:p.Arg1397Ser
|
|
XM_006724668.3:c.4470A>T
|
XP_006724731.1:p.Arg1490Ser
|
|
XM_017029601.2:c.4380A>T
|
XP_016885090.1:p.Arg1460Ser
|
|
XM_017029602.1:c.4350A>T
|
XP_016885091.1:p.Arg1450Ser
|
|
XM_017029603.1:c.4302A>T
|
XP_016885092.1:p.Arg1434Ser
|
|
XM_017029604.2:c.4269A>T
|
XP_016885093.1:p.Arg1423Ser
|
|
XM_017029605.1:c.4266A>T
|
XP_016885094.1:p.Arg1422Ser
|
|
XM_017029606.2:c.4239A>T
|
XP_016885095.1:p.Arg1413Ser
|
|
XM_017029607.2:c.4236A>T
|
XP_016885096.1:p.Arg1412Ser
|
|
XM_017029608.2:c.4188A>T
|
XP_016885097.1:p.Arg1396Ser
|
|
XM_017029609.1:c.4152A>T
|
XP_016885098.1:p.Arg1384Ser
|
|
XM_017029610.1:c.4149A>T
|
XP_016885099.1:p.Arg1383Ser
|
|
XM_017029611.1:c.4104A>T
|
XP_016885100.1:p.Arg1368Ser
|
|
XR_001755700.2:n.4695A>T
|
|
|
NM_138270.4:c.4356A>T
|
NP_612114.2:p.Arg1452Ser
|
|
NM_000489.6:c.4470A>T
MANE Select
|
NP_000480.3:p.Arg1490Ser
|
|
NM_138270.5:c.4356A>T
|
NP_612114.2:p.Arg1452Ser
|
|