ENST00000434651.7:c.*691G>T
MANE Select
|
ENSP00000407332.2:n.*691G>T
|
|
ENST00000374943.8:c.*691G>T
|
ENSP00000364080.4:n.*691G>T
|
|
ENST00000399079.7:c.*691G>T
|
ENSP00000382029.3:n.*691G>T
|
|
ENST00000399082.7:c.*691G>T
|
ENSP00000382032.3:n.*691G>T
|
|
ENST00000399084.5:c.*691G>T
|
ENSP00000382034.1:n.*691G>T
|
|
ENST00000434651.6:c.*691G>T
|
ENSP00000407332.2:n.*691G>T
|
|
ENST00000487676.1:n.4566G>T
|
|
|
NM_001243961.1:c.*691G>T
|
NP_001230890.1:n.*691G>T
|
|
NM_002123.4:c.*691G>T
|
NP_002114.3:n.*691G>T
|
|
NM_001243961.2:c.*691G>T
|
NP_001230890.1:n.*691G>T
|
|
NM_002123.5:c.*691G>T
MANE Select
|
NP_002114.3:n.*691G>T
|
|