NM_153329.4:c.1580C=
MANE Select
|
NP_699160.2:p.Pro527=
|
ENST00000293350.9:c.1580C=
MANE Select
|
ENSP00000293350.3:p.Pro527=
|
NM_001145396.1:c.1427C=
|
NP_001138868.1:p.Pro476=
|
NM_001145396.2:c.1427C=
|
NP_001138868.1:p.Pro476=
|
NM_153329.3:c.1580C=
|
NP_699160.2:p.Pro527=
|
ENST00000293350.8:c.1580C=
|
ENSP00000293350.3:p.Pro527=
|
ENST00000455361.6:c.1427C=
|
ENSP00000410142.1:p.Pro476=
|
ENST00000540132.5:c.1091C=
|
ENSP00000445088.1:p.Pro364=
|
ENST00000593417.5:c.*1038C=
|
ENSP00000470160.1:n.*1038C=
|
ENST00000599536.1:c.337+987C=
|
|
ENST00000599652.5:n.1758-32C=
|
|
ENST00000600265.1:c.227C=
|
ENSP00000469507.1:p.Pro76=
|
XM_011526441.1:c.1493C=
|
XP_011524743.1:p.Pro498=
|
XM_011526442.1:c.1493C=
|
XP_011524744.1:p.Pro498=
|