ENST00000373344.11:c.4514A>C
MANE Select
|
ENSP00000362441.4:p.Lys1505Thr
|
|
ENST00000373344.9:c.4514A>C
|
ENSP00000362441.4:p.Lys1505Thr
|
|
ENST00000395603.7:c.4400A>C
|
ENSP00000378967.3:p.Lys1467Thr
|
|
ENST00000480283.5:c.*4142A>C
|
ENSP00000480196.1:n.*4142A>C
|
|
ENST00000623242.3:c.120A>C
|
|
|
NM_000489.4:c.4514A>C
|
NP_000480.3:p.Lys1505Thr
|
|
NM_138270.3:c.4400A>C
|
NP_612114.2:p.Lys1467Thr
|
|
XM_005262153.3:c.4511A>C
|
XP_005262210.2:p.Lys1504Thr
|
|
XM_005262154.3:c.4427A>C
|
XP_005262211.2:p.Lys1476Thr
|
|
XM_005262155.3:c.4397A>C
|
XP_005262212.2:p.Lys1466Thr
|
|
XM_005262156.3:c.4349A>C
|
XP_005262213.2:p.Lys1450Thr
|
|
XM_005262157.3:c.4310A>C
|
XP_005262214.2:p.Lys1437Thr
|
|
XM_006724666.2:c.4397A>C
|
XP_006724729.1:p.Lys1466Thr
|
|
XM_006724667.2:c.4235A>C
|
XP_006724730.1:p.Lys1412Thr
|
|
XM_006724668.2:c.4514A>C
|
XP_006724731.1:p.Lys1505Thr
|
|
XR_938400.1:n.4782A>C
|
|
|
NM_000489.5:c.4514A>C
|
NP_000480.3:p.Lys1505Thr
|
|
XM_005262153.5:c.4511A>C
|
XP_005262210.2:p.Lys1504Thr
|
|
XM_005262154.5:c.4427A>C
|
XP_005262211.2:p.Lys1476Thr
|
|
XM_005262155.4:c.4397A>C
|
XP_005262212.2:p.Lys1466Thr
|
|
XM_005262156.4:c.4349A>C
|
XP_005262213.2:p.Lys1450Thr
|
|
XM_005262157.5:c.4310A>C
|
XP_005262214.2:p.Lys1437Thr
|
|
XM_006724666.4:c.4397A>C
|
XP_006724729.1:p.Lys1466Thr
|
|
XM_006724667.3:c.4235A>C
|
XP_006724730.1:p.Lys1412Thr
|
|
XM_006724668.3:c.4514A>C
|
XP_006724731.1:p.Lys1505Thr
|
|
XM_017029601.2:c.4424A>C
|
XP_016885090.1:p.Lys1475Thr
|
|
XM_017029602.1:c.4394A>C
|
XP_016885091.1:p.Lys1465Thr
|
|
XM_017029603.1:c.4346A>C
|
XP_016885092.1:p.Lys1449Thr
|
|
XM_017029604.2:c.4313A>C
|
XP_016885093.1:p.Lys1438Thr
|
|
XM_017029605.1:c.4310A>C
|
XP_016885094.1:p.Lys1437Thr
|
|
XM_017029606.2:c.4283A>C
|
XP_016885095.1:p.Lys1428Thr
|
|
XM_017029607.2:c.4280A>C
|
XP_016885096.1:p.Lys1427Thr
|
|
XM_017029608.2:c.4232A>C
|
XP_016885097.1:p.Lys1411Thr
|
|
XM_017029609.1:c.4196A>C
|
XP_016885098.1:p.Lys1399Thr
|
|
XM_017029610.1:c.4193A>C
|
XP_016885099.1:p.Lys1398Thr
|
|
XM_017029611.1:c.4148A>C
|
XP_016885100.1:p.Lys1383Thr
|
|
XR_001755700.2:n.4739A>C
|
|
|
NM_138270.4:c.4400A>C
|
NP_612114.2:p.Lys1467Thr
|
|
NM_000489.6:c.4514A>C
MANE Select
|
NP_000480.3:p.Lys1505Thr
|
|
NM_138270.5:c.4400A>C
|
NP_612114.2:p.Lys1467Thr
|
|