ENST00000436367.6:c.-615+11431G>C
MANE Select
|
ENSP00000416360.1:n.-615+11431G>C
|
|
ENST00000643828.1:n.344+11431G>C
|
|
|
ENST00000646259.1:n.188+11431G>C
|
|
|
ENST00000675689.1:n.150+11431G>C
|
|
|
ENST00000676138.1:n.162-1884G>C
|
|
|
ENST00000244769.8:c.-615+11431G>C
|
ENSP00000244769.3:n.-615+11431G>C
|
|
ENST00000436367.5:c.-615+11431G>C
|
ENSP00000416360.1:n.-615+11431G>C
|
|
ENST00000467008.5:n.295-1884G>C
|
|
|
ENST00000473388.6:n.278+11431G>C
|
|
|
ENST00000483591.6:n.117+8174G>C
|
|
|
ENST00000483954.1:n.159+19496G>C
|
|
|
ENST00000492857.1:n.331-1884G>C
|
|
|
ENST00000495178.1:n.76+11431G>C
|
|
|
ENST00000498374.1:n.195-1884G>C
|
|
|
NM_000332.3:c.-615+11431G>C
|
NP_000323.2:n.-615+11431G>C
|
|
NM_001128164.1:c.-615+11431G>C
|
NP_001121636.1:n.-615+11431G>C
|
|
NM_001357857.1:c.-644+11431G>C
|
NP_001344786.1:n.-644+11431G>C
|
|
NR_152111.1:n.309-1884G>C
|
|
|
NR_152112.1:n.194-1884G>C
|
|
|
NR_152113.1:n.191-1884G>C
|
|
|
NR_152114.1:n.240-1884G>C
|
|
|
NM_001357857.2:c.-644+11431G>C
|
NP_001344786.1:n.-644+11431G>C
|
|
NR_152111.2:n.279-1884G>C
|
|
|
NR_152112.2:n.164-1884G>C
|
|
|
NR_152113.2:n.244-1884G>C
|
|
|
NR_152114.2:n.293-1884G>C
|
|
|
NM_001128164.2:c.-615+11431G>C
MANE Select
|
NP_001121636.1:n.-615+11431G>C
|
|
NR_152111.3:n.279-1884G>C
|
|
|
NR_152112.3:n.164-1884G>C
|
|
|
NR_152113.3:n.244-1884G>C
|
|
|
NR_152114.3:n.293-1884G>C
|
|
|
NM_000332.4:c.-615+11431G>C
|
NP_000323.2:n.-615+11431G>C
|
|