ENST00000251810.8:c.*100G>T
MANE Select
|
ENSP00000251810.3:n.*100G>T
|
|
ENST00000251810.7:c.*100G>T
|
ENSP00000251810.3:n.*100G>T
|
|
ENST00000395910.6:n.543G>T
|
|
|
ENST00000522368.5:c.1325G>T
|
|
|
ENST00000621845.1:c.*100G>T
|
ENSP00000484318.1:n.*100G>T
|
|
NM_001172477.1:c.*100G>T , LRG_788t1:c.*100G>T
|
NP_001165948.1:n.*100G>T
|
|
NM_001172478.1:c.*100G>T
|
NP_001165949.1:n.*100G>T
|
|
NM_015713.4:c.*100G>T , LRG_788t2:c.*100G>T
|
NP_056528.2:n.*100G>T
|
|
NM_001172478.2:c.*100G>T
|
NP_001165949.1:n.*100G>T
|
|
NM_015713.5:c.*100G>T
MANE Select
|
NP_056528.2:n.*100G>T
|
|