ENST00000251810.8:c.*99T>C
MANE Select
|
ENSP00000251810.3:n.*99T>C
|
|
ENST00000251810.7:c.*99T>C
|
ENSP00000251810.3:n.*99T>C
|
|
ENST00000395910.6:n.542T>C
|
|
|
ENST00000522368.5:c.1324T>C
|
|
|
ENST00000621845.1:c.*99T>C
|
ENSP00000484318.1:n.*99T>C
|
|
NM_001172477.1:c.*99T>C , LRG_788t1:c.*99T>C
|
NP_001165948.1:n.*99T>C
|
|
NM_001172478.1:c.*99T>C
|
NP_001165949.1:n.*99T>C
|
|
NM_015713.4:c.*99T>C , LRG_788t2:c.*99T>C
|
NP_056528.2:n.*99T>C
|
|
NM_001172478.2:c.*99T>C
|
NP_001165949.1:n.*99T>C
|
|
NM_015713.5:c.*99T>C
MANE Select
|
NP_056528.2:n.*99T>C
|
|