ENST00000347901.9:c.1350T=
MANE Select
|
ENSP00000334002.4:p.Pro450=
|
|
ENST00000310778.5:c.1506T=
|
ENSP00000309392.5:p.Pro502=
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|
ENST00000341193.9:c.1299T=
|
ENSP00000343170.5:p.Pro433=
|
|
ENST00000347901.8:c.1350T=
|
ENSP00000334002.4:p.Pro450=
|
|
ENST00000393939.6:c.1275T=
|
ENSP00000377513.2:p.Pro425=
|
|
NM_001079870.1:c.1299T=
|
NP_001073339.1:p.Pro433=
|
|
NM_001079871.1:c.1275T=
|
NP_001073340.1:p.Pro425=
|
|
NM_177977.2:c.1350T=
|
NP_817084.2:p.Pro450=
|
|
NM_001367459.1:c.1446T=
|
NP_001354388.1:p.Pro482=
|
|
NM_001367460.1:c.1410T=
|
NP_001354389.1:p.Pro470=
|
|
NM_001367461.1:c.1275T=
|
NP_001354390.1:p.Pro425=
|
|
NM_001367462.1:c.1275T=
|
NP_001354391.1:p.Pro425=
|
|
NM_177977.3:c.1350T=
MANE Select
|
NP_817084.2:p.Pro450=
|
|