ENST00000367435.5:c.1030+197T>C
MANE Select
|
ENSP00000356405.4:n.1030+197T>C
|
|
ENST00000635846.1:c.787+197T>C
|
ENSP00000490035.1:n.787+197T>C
|
|
ENST00000643006.1:c.1098+197T>C
|
ENSP00000496633.1:n.1098+197T>C
|
|
ENST00000648071.1:c.*1006+197T>C
|
ENSP00000497513.1:n.*1006+197T>C
|
|
ENST00000649613.1:n.280+197T>C
|
|
|
ENST00000649895.1:n.1248+197T>C
|
|
|
ENST00000650197.1:c.1030+197T>C
|
ENSP00000496929.1:n.1030+197T>C
|
|
ENST00000367435.3:c.1030+197T>C
|
ENSP00000356405.3:n.1030+197T>C
|
|
NM_024529.4:c.1030+197T>C , LRG_507t1:c.1030+197T>C
|
NP_078805.3:n.1030+197T>C
|
|
NM_024529.5:c.1030+197T>C
MANE Select
|
NP_078805.3:n.1030+197T>C
|
|