ENST00000344327.8:c.945+241C>T
MANE Select
|
ENSP00000340913.3:n.945+241C>T
|
|
ENST00000344327.7:c.945+241C>T
|
ENSP00000340913.3:n.945+241C>T
|
|
ENST00000348423.8:c.945+241C>T
|
ENSP00000343672.4:n.945+241C>T
|
|
ENST00000360497.4:c.945+241C>T
|
ENSP00000353687.4:n.945+241C>T
|
|
ENST00000527240.1:n.67+241C>T
|
|
|
ENST00000532133.5:c.945+241C>T
|
ENSP00000435574.1:n.945+241C>T
|
|
NM_004621.5:c.945+241C>T
|
NP_004612.2:n.945+241C>T
|
|
XM_006718898.2:c.945+241C>T
|
XP_006718961.1:n.945+241C>T
|
|
XM_011542968.1:c.780+241C>T
|
XP_011541270.1:n.780+241C>T
|
|
XM_011542969.1:c.945+241C>T
|
XP_011541271.1:n.945+241C>T
|
|
XM_011542968.3:c.780+241C>T
|
XP_011541270.1:n.780+241C>T
|
|
XM_017018221.2:c.945+241C>T
|
XP_016873710.1:n.945+241C>T
|
|
XR_001747948.2:n.1301+241C>T
|
|
|
NM_004621.6:c.945+241C>T
MANE Select
|
NP_004612.2:n.945+241C>T
|
|