ENST00000281182.9:c.1195+353G>T
MANE Select
|
ENSP00000281182.5:n.1195+353G>T
|
|
ENST00000281182.8:c.1195+353G>T
|
ENSP00000281182.4:n.1195+353G>T
|
|
ENST00000374752.6:c.814+353G>T
|
ENSP00000363884.4:n.814+353G>T
|
|
ENST00000524502.2:n.401G>T
|
|
|
ENST00000531338.5:n.1792G>T
|
|
|
ENST00000533387.5:n.2254+353G>T
|
|
|
NM_014384.2:c.1195+353G>T , LRG_448t1:c.1195+353G>T
|
NP_055199.1:n.1195+353G>T
|
|
XM_005271501.2:c.*96G>T
|
XP_005271558.1:n.*96G>T
|
|
XM_011542750.1:c.1195+353G>T
|
XP_011541052.1:n.1195+353G>T
|
|
XR_947819.1:n.1259+353G>T
|
|
|
XR_947820.1:n.2000G>T
|
|
|
XR_947822.1:n.1089+353G>T
|
|
|
XR_947823.1:n.1245+353G>T
|
|
|
XM_005271505.4:c.*1460+353G>T
|
XP_005271562.1:n.*1460+353G>T
|
|
XM_011542750.3:c.1195+353G>T
|
XP_011541052.1:n.1195+353G>T
|
|
XM_017017542.2:c.1195+353G>T
|
XP_016873031.1:n.1195+353G>T
|
|
XM_017017543.2:c.*96G>T
|
XP_016873032.1:n.*96G>T
|
|
XM_017017544.2:c.*164+353G>T
|
XP_016873033.1:n.*164+353G>T
|
|
XM_017017545.2:c.*760G>T
|
XP_016873034.1:n.*760G>T
|
|
XM_017017546.2:c.901+353G>T
|
XP_016873035.1:n.901+353G>T
|
|
XM_017017547.2:c.901+353G>T
|
XP_016873036.1:n.901+353G>T
|
|
XM_017017548.2:c.*2037G>T
|
XP_016873037.1:n.*2037G>T
|
|
XM_017017549.2:c.*1605+353G>T
|
XP_016873038.1:n.*1605+353G>T
|
|
XM_024448437.1:c.*695G>T
|
XP_024304205.1:n.*695G>T
|
|
XM_024448438.1:c.814+353G>T
|
XP_024304206.1:n.814+353G>T
|
|
NM_014384.3:c.1195+353G>T
MANE Select
|
NP_055199.1:n.1195+353G>T
|
|