ENST00000304046.7:c.-23+1389G>T
MANE Select
|
ENSP00000304858.2:n.-23+1389G>T
|
|
ENST00000304046.6:c.-23+1389G>T
|
ENSP00000304858.2:n.-23+1389G>T
|
|
ENST00000394169.5:c.-749G>T
|
ENSP00000377724.1:n.-749G>T
|
|
ENST00000579695.5:c.-18+1389G>T
|
ENSP00000464693.1:n.-18+1389G>T
|
|
ENST00000582052.1:n.275G>T
|
|
|
ENST00000584000.1:c.-23+972G>T
|
ENSP00000464298.1:n.-23+972G>T
|
|
NM_139280.2:c.-23+1389G>T
|
NP_644809.1:n.-23+1389G>T
|
|
XM_005257825.3:c.-23+722G>T
|
XP_005257882.2:n.-23+722G>T
|
|
XM_005257827.2:c.-18+1389G>T
|
XP_005257884.1:n.-18+1389G>T
|
|
NM_001320801.1:c.-749G>T
|
NP_001307730.1:n.-749G>T
|
|
NM_001320802.1:c.-18+1389G>T
|
NP_001307731.1:n.-18+1389G>T
|
|
NM_001320803.1:c.-23+722G>T
|
NP_001307732.1:n.-23+722G>T
|
|
NM_139280.3:c.-23+1389G>T
|
NP_644809.1:n.-23+1389G>T
|
|
NM_139280.4:c.-23+1389G>T
MANE Select
|
NP_644809.1:n.-23+1389G>T
|
|
NM_001320802.2:c.-18+1389G>T
|
NP_001307731.1:n.-18+1389G>T
|
|
NM_001320801.2:c.-749G>T
|
NP_001307730.1:n.-749G>T
|
|