ENST00000373344.11:c.4448T>C
MANE Select
|
ENSP00000362441.4:p.Ile1483Thr
|
|
ENST00000373344.9:c.4448T>C
|
ENSP00000362441.4:p.Ile1483Thr
|
|
ENST00000395603.7:c.4334T>C
|
ENSP00000378967.3:p.Ile1445Thr
|
|
ENST00000480283.5:c.*4076T>C
|
ENSP00000480196.1:n.*4076T>C
|
|
ENST00000623242.3:c.54T>C
|
|
|
NM_000489.4:c.4448T>C
|
NP_000480.3:p.Ile1483Thr
|
|
NM_138270.3:c.4334T>C
|
NP_612114.2:p.Ile1445Thr
|
|
XM_005262153.3:c.4445T>C
|
XP_005262210.2:p.Ile1482Thr
|
|
XM_005262154.3:c.4361T>C
|
XP_005262211.2:p.Ile1454Thr
|
|
XM_005262155.3:c.4331T>C
|
XP_005262212.2:p.Ile1444Thr
|
|
XM_005262156.3:c.4283T>C
|
XP_005262213.2:p.Ile1428Thr
|
|
XM_005262157.3:c.4244T>C
|
XP_005262214.2:p.Ile1415Thr
|
|
XM_006724666.2:c.4331T>C
|
XP_006724729.1:p.Ile1444Thr
|
|
XM_006724667.2:c.4169T>C
|
XP_006724730.1:p.Ile1390Thr
|
|
XM_006724668.2:c.4448T>C
|
XP_006724731.1:p.Ile1483Thr
|
|
XR_938400.1:n.4716T>C
|
|
|
NM_000489.5:c.4448T>C
|
NP_000480.3:p.Ile1483Thr
|
|
XM_005262153.5:c.4445T>C
|
XP_005262210.2:p.Ile1482Thr
|
|
XM_005262154.5:c.4361T>C
|
XP_005262211.2:p.Ile1454Thr
|
|
XM_005262155.4:c.4331T>C
|
XP_005262212.2:p.Ile1444Thr
|
|
XM_005262156.4:c.4283T>C
|
XP_005262213.2:p.Ile1428Thr
|
|
XM_005262157.5:c.4244T>C
|
XP_005262214.2:p.Ile1415Thr
|
|
XM_006724666.4:c.4331T>C
|
XP_006724729.1:p.Ile1444Thr
|
|
XM_006724667.3:c.4169T>C
|
XP_006724730.1:p.Ile1390Thr
|
|
XM_006724668.3:c.4448T>C
|
XP_006724731.1:p.Ile1483Thr
|
|
XM_017029601.2:c.4358T>C
|
XP_016885090.1:p.Ile1453Thr
|
|
XM_017029602.1:c.4328T>C
|
XP_016885091.1:p.Ile1443Thr
|
|
XM_017029603.1:c.4280T>C
|
XP_016885092.1:p.Ile1427Thr
|
|
XM_017029604.2:c.4247T>C
|
XP_016885093.1:p.Ile1416Thr
|
|
XM_017029605.1:c.4244T>C
|
XP_016885094.1:p.Ile1415Thr
|
|
XM_017029606.2:c.4217T>C
|
XP_016885095.1:p.Ile1406Thr
|
|
XM_017029607.2:c.4214T>C
|
XP_016885096.1:p.Ile1405Thr
|
|
XM_017029608.2:c.4166T>C
|
XP_016885097.1:p.Ile1389Thr
|
|
XM_017029609.1:c.4130T>C
|
XP_016885098.1:p.Ile1377Thr
|
|
XM_017029610.1:c.4127T>C
|
XP_016885099.1:p.Ile1376Thr
|
|
XM_017029611.1:c.4082T>C
|
XP_016885100.1:p.Ile1361Thr
|
|
XR_001755700.2:n.4673T>C
|
|
|
NM_138270.4:c.4334T>C
|
NP_612114.2:p.Ile1445Thr
|
|
NM_000489.6:c.4448T>C
MANE Select
|
NP_000480.3:p.Ile1483Thr
|
|
NM_138270.5:c.4334T>C
|
NP_612114.2:p.Ile1445Thr
|
|