ENST00000691062.1:c.3945T=
MANE Select
|
ENSP00000510348.1:p.Ser1315=
|
|
ENST00000402510.2:c.4473T=
|
ENSP00000384670.2:p.Ser1491=
|
|
NM_020721.1:c.4473T=
|
NP_065772.1:p.Ser1491=
|
|
XM_006724774.2:c.3945T=
|
XP_006724837.1:p.Ser1315=
|
|
XM_011531375.1:c.3747T=
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XP_011529677.1:p.Ser1249=
|
|
XM_006724774.3:c.3945T=
|
XP_006724837.1:p.Ser1315=
|
|
XM_017029688.2:c.3990T=
|
XP_016885177.1:p.Ser1330=
|
|
XM_017029689.2:c.3792T=
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XP_016885178.1:p.Ser1264=
|
|
XM_024452412.1:c.3747T=
|
XP_024308180.1:p.Ser1249=
|
|
NM_001394962.1:c.3945T=
MANE Select
|
NP_001381891.1:p.Ser1315=
|
|