ENST00000481739.2:c.610+811T>C
MANE Select
|
ENSP00000419692.1:n.610+811T>C
|
|
ENST00000672570.1:c.529+811T>C
|
ENSP00000500402.1:n.529+811T>C
|
|
ENST00000356384.4:n.1020+811T>C
|
|
|
ENST00000481739.1:c.610+811T>C
|
ENSP00000419692.1:n.610+811T>C
|
|
NM_001291920.1:c.529+811T>C
|
NP_001278849.1:n.529+811T>C
|
|
NM_001291921.1:c.319+811T>C
|
NP_001278850.1:n.319+811T>C
|
|
NM_002957.5:c.610+811T>C
|
NP_002948.1:n.610+811T>C
|
|
NM_002957.6:c.610+811T>C
MANE Select
|
NP_002948.1:n.610+811T>C
|
|
NM_001291921.2:c.319+811T>C
|
NP_001278850.1:n.319+811T>C
|
|
NM_001291920.2:c.529+811T>C
|
NP_001278849.1:n.529+811T>C
|
|