ENST00000424848.3:c.*7625T>A
MANE Select
|
ENSP00000397087.3:n.*7625T>A
|
|
ENST00000265734.8:c.*7625T>A
|
ENSP00000265734.4:n.*7625T>A
|
|
NM_001145306.1:c.*7625T>A
|
NP_001138778.1:n.*7625T>A
|
|
NM_001259.6:c.*7625T>A
|
NP_001250.1:n.*7625T>A
|
|
XM_006715835.1:c.*7625T>A
|
XP_006715898.1:n.*7625T>A
|
|
XM_011515731.1:c.*7625T>A
|
XP_011514033.1:n.*7625T>A
|
|
NM_001259.7:c.*7625T>A
|
NP_001250.1:n.*7625T>A
|
|
XM_006715835.2:c.*7625T>A
|
XP_006715898.1:n.*7625T>A
|
|
NM_001145306.2:c.*7625T>A
MANE Select
|
NP_001138778.1:n.*7625T>A
|
|
NM_001259.8:c.*7625T>A
|
NP_001250.1:n.*7625T>A
|
|