ENST00000305188.13:c.*222T>C
MANE Select
|
ENSP00000306999.8:n.*222T>C
|
|
ENST00000305188.12:c.*222T>C
|
ENSP00000306999.8:n.*222T>C
|
|
ENST00000397418.4:c.685+287T>C
|
ENSP00000380563.2:n.685+287T>C
|
|
ENST00000522378.5:c.*716+287T>C
|
ENSP00000428928.1:n.*716+287T>C
|
|
NM_001017420.2:c.*222T>C
|
NP_001017420.1:n.*222T>C
|
|
XM_011544421.1:c.*222T>C
|
XP_011542723.1:n.*222T>C
|
|
XM_011544422.1:c.1741+287T>C
|
XP_011542724.1:n.1741+287T>C
|
|
XR_949378.1:n.1825+287T>C
|
|
|
XR_949379.1:n.1825+287T>C
|
|
|
XM_011544421.2:c.*222T>C
|
XP_011542723.1:n.*222T>C
|
|
XM_011544422.2:c.1741+287T>C
|
XP_011542724.1:n.1741+287T>C
|
|
XR_949378.3:n.1825+287T>C
|
|
|
NM_001017420.3:c.*222T>C
MANE Select
|
NP_001017420.1:n.*222T>C
|
|