ENST00000244741.10:c.-6+2091T>C
MANE Select
|
ENSP00000244741.6:n.-6+2091T>C
|
|
ENST00000244741.9:c.-6+2091T>C
|
ENSP00000244741.5:n.-6+2091T>C
|
|
ENST00000373711.3:c.-96-1751T>C
|
ENSP00000362815.1:n.-96-1751T>C
|
|
ENST00000405375.5:c.-6+1950T>C
|
ENSP00000384849.1:n.-6+1950T>C
|
|
ENST00000448526.6:c.-6+2956T>C
|
ENSP00000409259.3:n.-6+2956T>C
|
|
ENST00000459970.1:n.189+2956T>C
|
|
|
ENST00000478800.1:n.214+1950T>C
|
|
|
ENST00000615513.4:c.-5-3208T>C
|
ENSP00000482768.1:n.-5-3208T>C
|
|
NM_000389.4:c.-6+2091T>C
|
NP_000380.1:n.-6+2091T>C
|
|
NM_001220777.1:c.-5-3208T>C
|
NP_001207706.1:n.-5-3208T>C
|
|
NM_001220778.1:c.-6+1950T>C
|
NP_001207707.1:n.-6+1950T>C
|
|
NM_001291549.1:c.97+2956T>C
|
NP_001278478.1:n.97+2956T>C
|
|
NM_078467.2:c.-6+2956T>C
|
NP_510867.1:n.-6+2956T>C
|
|
XM_011515041.1:c.*35T>C
|
XP_011513343.1:n.*35T>C
|
|
NM_000389.5:c.-6+2091T>C
MANE Select
|
NP_000380.1:n.-6+2091T>C
|
|
NM_001220777.2:c.-5-3208T>C
|
NP_001207706.1:n.-5-3208T>C
|
|
NM_001220778.2:c.-6+1950T>C
|
NP_001207707.1:n.-6+1950T>C
|
|
NM_001291549.3:c.97+2956T>C
|
NP_001278478.1:n.97+2956T>C
|
|
NM_001374509.1:c.97+2956T>C
|
NP_001361438.1:n.97+2956T>C
|
|
NM_001374510.1:c.35-3208T>C
|
NP_001361439.1:n.35-3208T>C
|
|
NM_001374511.1:c.-6+2091T>C
|
NP_001361440.1:n.-6+2091T>C
|
|
NM_001374512.1:c.-6+2091T>C
|
NP_001361441.1:n.-6+2091T>C
|
|
NM_001374513.1:c.-6+1984T>C
|
NP_001361442.1:n.-6+1984T>C
|
|
NM_078467.3:c.-6+2956T>C
|
NP_510867.1:n.-6+2956T>C
|
|