ENST00000281182.9:c.1195+152G>T
MANE Select
|
ENSP00000281182.5:n.1195+152G>T
|
|
ENST00000281182.8:c.1195+152G>T
|
ENSP00000281182.4:n.1195+152G>T
|
|
ENST00000374752.6:c.814+152G>T
|
ENSP00000363884.4:n.814+152G>T
|
|
ENST00000524502.2:n.200G>T
|
|
|
ENST00000526026.5:c.*889G>T
|
ENSP00000431532.1:n.*889G>T
|
|
ENST00000531338.5:n.1591G>T
|
|
|
ENST00000533387.5:n.2254+152G>T
|
|
|
NM_014384.2:c.1195+152G>T , LRG_448t1:c.1195+152G>T
|
NP_055199.1:n.1195+152G>T
|
|
XM_005271501.2:c.1200G>T
|
XP_005271558.1:p.Leu400=
|
|
XM_011542750.1:c.1195+152G>T
|
XP_011541052.1:n.1195+152G>T
|
|
XR_947819.1:n.1259+152G>T
|
|
|
XR_947820.1:n.1799G>T
|
|
|
XR_947822.1:n.1089+152G>T
|
|
|
XR_947823.1:n.1245+152G>T
|
|
|
XM_005271505.4:c.*1460+152G>T
|
XP_005271562.1:n.*1460+152G>T
|
|
XM_011542750.3:c.1195+152G>T
|
XP_011541052.1:n.1195+152G>T
|
|
XM_017017542.2:c.1195+152G>T
|
XP_016873031.1:n.1195+152G>T
|
|
XM_017017543.2:c.1200G>T
|
XP_016873032.1:p.Leu400=
|
|
XM_017017544.2:c.*164+152G>T
|
XP_016873033.1:n.*164+152G>T
|
|
XM_017017545.2:c.*559G>T
|
XP_016873034.1:n.*559G>T
|
|
XM_017017546.2:c.901+152G>T
|
XP_016873035.1:n.901+152G>T
|
|
XM_017017547.2:c.901+152G>T
|
XP_016873036.1:n.901+152G>T
|
|
XM_017017548.2:c.*1836G>T
|
XP_016873037.1:n.*1836G>T
|
|
XM_017017549.2:c.*1605+152G>T
|
XP_016873038.1:n.*1605+152G>T
|
|
XM_024448437.1:c.*494G>T
|
XP_024304205.1:n.*494G>T
|
|
XM_024448438.1:c.814+152G>T
|
XP_024304206.1:n.814+152G>T
|
|
NM_014384.3:c.1195+152G>T
MANE Select
|
NP_055199.1:n.1195+152G>T
|
|