ENST00000534010.2:c.314+6316T>A
|
ENSP00000433202.2:n.314+6316T>A
|
|
ENST00000375549.8:c.*357T>A
MANE Select
|
ENSP00000364699.3:n.*357T>A
|
|
ENST00000528021.6:c.314+6316T>A
|
ENSP00000432465.1:n.314+6316T>A
|
|
ENST00000375549.7:c.*357T>A
|
ENSP00000364699.3:n.*357T>A
|
|
ENST00000525291.5:c.*357T>A
|
ENSP00000436669.1:n.*357T>A
|
|
ENST00000525987.5:n.319+6316T>A
|
|
|
ENST00000528021.5:c.314+6316T>A
|
ENSP00000432465.1:n.314+6316T>A
|
|
ENST00000528048.5:c.*434T>A
|
ENSP00000436217.1:n.*434T>A
|
|
ENST00000531744.5:c.314+6316T>A
|
ENSP00000456957.1:n.314+6316T>A
|
|
ENST00000532699.1:c.314+6316T>A
|
ENSP00000456434.1:n.314+6316T>A
|
|
ENST00000534010.1:c.145+6316T>A
|
|
|
NM_001276503.1:c.*434T>A
|
NP_001263432.1:n.*434T>A
|
|
NM_001276504.1:c.*357T>A
|
NP_001263433.1:n.*357T>A
|
|
NM_001276506.1:c.*535T>A
|
NP_001263435.1:n.*535T>A
|
|
NM_003002.3:c.*357T>A
|
NP_002993.1:n.*357T>A
|
|
NR_077060.1:n.975T>A
|
|
|
NM_003002.4:c.*357T>A
MANE Select
|
NP_002993.1:n.*357T>A
|
|
NM_001276503.2:c.*434T>A
|
NP_001263432.1:n.*434T>A
|
|
NM_001276504.2:c.*357T>A
|
NP_001263433.1:n.*357T>A
|
|
NM_001276506.2:c.*535T>A
|
NP_001263435.1:n.*535T>A
|
|
NR_077060.2:n.926T>A
|
|
|