ENST00000344327.8:c.1293+176A>T
MANE Select
|
ENSP00000340913.3:n.1293+176A>T
|
|
ENST00000344327.7:c.1293+176A>T
|
ENSP00000340913.3:n.1293+176A>T
|
|
ENST00000348423.8:c.946-5596A>T
|
ENSP00000343672.4:n.946-5596A>T
|
|
ENST00000360497.4:c.1128+2795A>T
|
ENSP00000353687.4:n.1128+2795A>T
|
|
ENST00000532133.5:c.1293+176A>T
|
ENSP00000435574.1:n.1293+176A>T
|
|
NM_004621.5:c.1293+176A>T
|
NP_004612.2:n.1293+176A>T
|
|
XM_006718898.2:c.1293+176A>T
|
XP_006718961.1:n.1293+176A>T
|
|
XM_011542968.1:c.1128+176A>T
|
XP_011541270.1:n.1128+176A>T
|
|
XM_011542969.1:c.1293+176A>T
|
XP_011541271.1:n.1293+176A>T
|
|
XM_011542968.3:c.1128+176A>T
|
XP_011541270.1:n.1128+176A>T
|
|
XM_017018221.2:c.946-5596A>T
|
XP_016873710.1:n.946-5596A>T
|
|
XR_001747948.2:n.1649+176A>T
|
|
|
NM_004621.6:c.1293+176A>T
MANE Select
|
NP_004612.2:n.1293+176A>T
|
|