ENST00000542639.6:c.1038+11T>C
|
ENSP00000440846.1:n.1038+11T>C
|
|
ENST00000686683.1:c.747+11T>C
|
ENSP00000509063.1:n.747+11T>C
|
|
ENST00000686980.1:n.5969+11T>C
|
|
|
ENST00000688006.1:c.1038+11T>C
|
ENSP00000510311.1:n.1038+11T>C
|
|
ENST00000688859.1:n.993+11T>C
|
|
|
ENST00000689087.1:c.1038+11T>C
|
ENSP00000508997.1:n.1038+11T>C
|
|
ENST00000693128.1:c.1332+11T>C
|
ENSP00000508493.1:n.1332+11T>C
|
|
ENST00000338702.4:c.1437+11T>C
MANE Select
|
ENSP00000340684.3:n.1437+11T>C
|
|
ENST00000338702.3:c.1437+11T>C
|
ENSP00000340684.3:n.1437+11T>C
|
|
ENST00000490604.1:n.265+11T>C
|
|
|
ENST00000542639.5:c.1038+11T>C
|
ENSP00000440846.1:n.1038+11T>C
|
|
NM_000240.3:c.1437+11T>C
|
NP_000231.1:n.1437+11T>C
|
|
NM_001270458.1:c.1038+11T>C
|
NP_001257387.1:n.1038+11T>C
|
|
NM_000240.4:c.1437+11T>C
MANE Select
|
NP_000231.1:n.1437+11T>C
|
|
NM_001270458.2:c.1038+11T>C
|
NP_001257387.1:n.1038+11T>C
|
|