ENST00000437033.7:c.825+186G>C
MANE Select
|
ENSP00000414254.2:n.825+186G>C
|
|
ENST00000209665.8:c.861+186G>C
|
ENSP00000209665.4:n.861+186G>C
|
|
ENST00000437033.6:c.825+186G>C
|
ENSP00000414254.2:n.825+186G>C
|
|
ENST00000476959.5:c.885+186G>C
|
ENSP00000420269.1:n.885+186G>C
|
|
ENST00000482593.5:c.654+186G>C
|
ENSP00000420613.1:n.654+186G>C
|
|
NM_000673.4:c.861+186G>C
|
NP_000664.2:n.861+186G>C
|
|
NM_001166504.1:c.885+186G>C
|
NP_001159976.1:n.885+186G>C
|
|
NM_000673.7:c.825+186G>C
MANE Select
|
NP_000664.3:n.825+186G>C
|
|
NM_001166504.2:c.885+186G>C
|
NP_001159976.1:n.885+186G>C
|
|