ENST00000343139.11:c.423T>C
MANE Select
|
ENSP00000339398.5:p.Pro141=
|
|
ENST00000343139.9:c.423T>C
|
ENSP00000339398.5:p.Pro141=
|
|
ENST00000374949.2:c.423T>C
|
ENSP00000364087.2:p.Pro141=
|
|
ENST00000395363.5:c.423T>C
|
ENSP00000378767.1:p.Pro141=
|
|
ENST00000460633.1:n.451T>C
|
|
|
ENST00000482745.5:c.*1255T>C
|
ENSP00000436546.1:n.*1255T>C
|
|
ENST00000496318.5:c.423T>C
|
ENSP00000437302.1:p.Pro141=
|
|
NM_002122.3:c.423T>C
|
NP_002113.2:p.Pro141=
|
|
XM_006715079.2:c.423T>C
|
XP_006715142.1:p.Pro141=
|
|
XM_006715079.4:c.423T>C
|
XP_006715142.1:p.Pro141=
|
|
XR_001744085.1:n.86+525A>G
|
|
|
NM_002122.5:c.423T>C
MANE Select
|
NP_002113.2:p.Pro141=
|
|