ENST00000373344.11:c.4395T=
MANE Select
|
ENSP00000362441.4:p.Asp1465=
|
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ENST00000373344.9:c.4395T=
|
ENSP00000362441.4:p.Asp1465=
|
|
ENST00000395603.7:c.4281T=
|
ENSP00000378967.3:p.Asp1427=
|
|
ENST00000480283.5:c.*4023T=
|
ENSP00000480196.1:n.*4023T=
|
|
ENST00000623242.3:c.1T=
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|
|
NM_000489.4:c.4395T=
|
NP_000480.3:p.Asp1465=
|
|
NM_138270.3:c.4281T=
|
NP_612114.2:p.Asp1427=
|
|
XM_005262153.3:c.4392T=
|
XP_005262210.2:p.Asp1464=
|
|
XM_005262154.3:c.4308T=
|
XP_005262211.2:p.Asp1436=
|
|
XM_005262155.3:c.4278T=
|
XP_005262212.2:p.Asp1426=
|
|
XM_005262156.3:c.4230T=
|
XP_005262213.2:p.Asp1410=
|
|
XM_005262157.3:c.4191T=
|
XP_005262214.2:p.Asp1397=
|
|
XM_006724666.2:c.4278T=
|
XP_006724729.1:p.Asp1426=
|
|
XM_006724667.2:c.4116T=
|
XP_006724730.1:p.Asp1372=
|
|
XM_006724668.2:c.4395T=
|
XP_006724731.1:p.Asp1465=
|
|
XR_938400.1:n.4663T=
|
|
|
NM_000489.5:c.4395T=
|
NP_000480.3:p.Asp1465=
|
|
XM_005262153.5:c.4392T=
|
XP_005262210.2:p.Asp1464=
|
|
XM_005262154.5:c.4308T=
|
XP_005262211.2:p.Asp1436=
|
|
XM_005262155.4:c.4278T=
|
XP_005262212.2:p.Asp1426=
|
|
XM_005262156.4:c.4230T=
|
XP_005262213.2:p.Asp1410=
|
|
XM_005262157.5:c.4191T=
|
XP_005262214.2:p.Asp1397=
|
|
XM_006724666.4:c.4278T=
|
XP_006724729.1:p.Asp1426=
|
|
XM_006724667.3:c.4116T=
|
XP_006724730.1:p.Asp1372=
|
|
XM_006724668.3:c.4395T=
|
XP_006724731.1:p.Asp1465=
|
|
XM_017029601.2:c.4305T=
|
XP_016885090.1:p.Asp1435=
|
|
XM_017029602.1:c.4275T=
|
XP_016885091.1:p.Asp1425=
|
|
XM_017029603.1:c.4227T=
|
XP_016885092.1:p.Asp1409=
|
|
XM_017029604.2:c.4194T=
|
XP_016885093.1:p.Asp1398=
|
|
XM_017029605.1:c.4191T=
|
XP_016885094.1:p.Asp1397=
|
|
XM_017029606.2:c.4164T=
|
XP_016885095.1:p.Asp1388=
|
|
XM_017029607.2:c.4161T=
|
XP_016885096.1:p.Asp1387=
|
|
XM_017029608.2:c.4113T=
|
XP_016885097.1:p.Asp1371=
|
|
XM_017029609.1:c.4077T=
|
XP_016885098.1:p.Asp1359=
|
|
XM_017029610.1:c.4074T=
|
XP_016885099.1:p.Asp1358=
|
|
XM_017029611.1:c.4029T=
|
XP_016885100.1:p.Asp1343=
|
|
XR_001755700.2:n.4620T=
|
|
|
NM_138270.4:c.4281T=
|
NP_612114.2:p.Asp1427=
|
|
NM_000489.6:c.4395T=
MANE Select
|
NP_000480.3:p.Asp1465=
|
|
NM_138270.5:c.4281T=
|
NP_612114.2:p.Asp1427=
|
|