ENST00000373344.11:c.4371G>A
MANE Select
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ENSP00000362441.4:p.Glu1457=
|
|
ENST00000373344.9:c.4371G>A
|
ENSP00000362441.4:p.Glu1457=
|
|
ENST00000395603.7:c.4257G>A
|
ENSP00000378967.3:p.Glu1419=
|
|
ENST00000480283.5:c.*3999G>A
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ENSP00000480196.1:n.*3999G>A
|
|
NM_000489.4:c.4371G>A
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NP_000480.3:p.Glu1457=
|
|
NM_138270.3:c.4257G>A
|
NP_612114.2:p.Glu1419=
|
|
XM_005262153.3:c.4368G>A
|
XP_005262210.2:p.Glu1456=
|
|
XM_005262154.3:c.4284G>A
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XP_005262211.2:p.Glu1428=
|
|
XM_005262155.3:c.4254G>A
|
XP_005262212.2:p.Glu1418=
|
|
XM_005262156.3:c.4206G>A
|
XP_005262213.2:p.Glu1402=
|
|
XM_005262157.3:c.4167G>A
|
XP_005262214.2:p.Glu1389=
|
|
XM_006724666.2:c.4254G>A
|
XP_006724729.1:p.Glu1418=
|
|
XM_006724667.2:c.4092G>A
|
XP_006724730.1:p.Glu1364=
|
|
XM_006724668.2:c.4371G>A
|
XP_006724731.1:p.Glu1457=
|
|
XR_938400.1:n.4639G>A
|
|
|
NM_000489.5:c.4371G>A
|
NP_000480.3:p.Glu1457=
|
|
XM_005262153.5:c.4368G>A
|
XP_005262210.2:p.Glu1456=
|
|
XM_005262154.5:c.4284G>A
|
XP_005262211.2:p.Glu1428=
|
|
XM_005262155.4:c.4254G>A
|
XP_005262212.2:p.Glu1418=
|
|
XM_005262156.4:c.4206G>A
|
XP_005262213.2:p.Glu1402=
|
|
XM_005262157.5:c.4167G>A
|
XP_005262214.2:p.Glu1389=
|
|
XM_006724666.4:c.4254G>A
|
XP_006724729.1:p.Glu1418=
|
|
XM_006724667.3:c.4092G>A
|
XP_006724730.1:p.Glu1364=
|
|
XM_006724668.3:c.4371G>A
|
XP_006724731.1:p.Glu1457=
|
|
XM_017029601.2:c.4281G>A
|
XP_016885090.1:p.Glu1427=
|
|
XM_017029602.1:c.4251G>A
|
XP_016885091.1:p.Glu1417=
|
|
XM_017029603.1:c.4203G>A
|
XP_016885092.1:p.Glu1401=
|
|
XM_017029604.2:c.4170G>A
|
XP_016885093.1:p.Glu1390=
|
|
XM_017029605.1:c.4167G>A
|
XP_016885094.1:p.Glu1389=
|
|
XM_017029606.2:c.4140G>A
|
XP_016885095.1:p.Glu1380=
|
|
XM_017029607.2:c.4137G>A
|
XP_016885096.1:p.Glu1379=
|
|
XM_017029608.2:c.4089G>A
|
XP_016885097.1:p.Glu1363=
|
|
XM_017029609.1:c.4053G>A
|
XP_016885098.1:p.Glu1351=
|
|
XM_017029610.1:c.4050G>A
|
XP_016885099.1:p.Glu1350=
|
|
XM_017029611.1:c.4005G>A
|
XP_016885100.1:p.Glu1335=
|
|
XR_001755700.2:n.4596G>A
|
|
|
NM_138270.4:c.4257G>A
|
NP_612114.2:p.Glu1419=
|
|
NM_000489.6:c.4371G>A
MANE Select
|
NP_000480.3:p.Glu1457=
|
|
NM_138270.5:c.4257G>A
|
NP_612114.2:p.Glu1419=
|
|