ENST00000383032.6:c.-140+7558G>T
MANE Select
|
ENSP00000372499.1:n.-140+7558G>T
|
|
ENST00000346432.3:c.-139-17993G>T
|
ENSP00000328879.4:n.-139-17993G>T
|
|
ENST00000355162.6:c.-140+7558G>T
|
ENSP00000347289.2:n.-140+7558G>T
|
|
ENST00000383032.5:c.-140+7558G>T
|
ENSP00000372499.1:n.-140+7558G>T
|
|
NM_033284.1:c.-140+7558G>T
|
NP_150600.1:n.-140+7558G>T
|
|
NM_134258.1:c.-140+7558G>T
|
NP_599020.1:n.-140+7558G>T
|
|
NM_134259.1:c.-139-17993G>T
|
NP_599021.1:n.-139-17993G>T
|
|
XM_017030086.1:c.-140+7558G>T
|
XP_016885575.1:n.-140+7558G>T
|
|
XM_017030087.1:c.-140+7558G>T
|
XP_016885576.1:n.-140+7558G>T
|
|
XM_024452497.1:c.-140+7558G>T
|
XP_024308265.1:n.-140+7558G>T
|
|
NM_033284.2:c.-140+7558G>T
MANE Select
|
NP_150600.1:n.-140+7558G>T
|
|
NM_134258.2:c.-140+7558G>T
|
NP_599020.1:n.-140+7558G>T
|
|
NM_134259.2:c.-139-17993G>T
|
NP_599021.1:n.-139-17993G>T
|
|