|
ENST00000392017.9:c.954+127T>C
MANE Select
|
ENSP00000375872.4:n.954+127T>C
|
|
|
ENST00000347464.9:c.465+127T>C
|
ENSP00000318259.6:n.465+127T>C
|
|
|
ENST00000373525.9:c.522+127T>C
|
ENSP00000362625.5:n.522+127T>C
|
|
|
ENST00000392017.8:c.954+127T>C
|
ENSP00000375872.4:n.954+127T>C
|
|
|
ENST00000392018.1:c.1005+127T>C
|
ENSP00000375873.1:n.1005+127T>C
|
|
|
ENST00000392020.8:c.897+127T>C
|
ENSP00000375875.4:n.897+127T>C
|
|
|
ENST00000392021.7:c.*835+127T>C
|
ENSP00000375876.3:n.*835+127T>C
|
|
|
ENST00000419681.5:c.465+127T>C
|
ENSP00000398773.1:n.465+127T>C
|
|
|
ENST00000474148.5:n.1749+127T>C
|
|
|
|
ENST00000479942.5:n.1100+127T>C
|
|
|
|
ENST00000492298.5:n.475+127T>C
|
|
|
|
ENST00000498620.5:n.461+127T>C
|
|
|
|
NM_001190266.1:c.702+127T>C
|
NP_001177195.1:n.702+127T>C
|
|
|
NM_001190267.1:c.606+127T>C
|
NP_001177196.1:n.606+127T>C
|
|
|
NM_017974.3:c.897+127T>C
|
NP_060444.3:n.897+127T>C
|
|
|
NM_030803.6:c.954+127T>C
|
NP_110430.5:n.954+127T>C
|
|
|
NM_198890.2:c.465+127T>C
|
NP_942593.2:n.465+127T>C
|
|
|
XM_005246082.1:c.1005+127T>C
|
XP_005246139.1:n.1005+127T>C
|
|
|
XM_005246084.1:c.573+127T>C
|
XP_005246141.1:n.573+127T>C
|
|
|
XM_005246086.1:c.522+127T>C
|
XP_005246143.1:n.522+127T>C
|
|
|
XM_006712608.1:c.753+127T>C
|
XP_006712671.1:n.753+127T>C
|
|
|
XR_241242.1:n.1199+127T>C
|
|
|
|
NM_001363742.1:c.1005+127T>C
|
NP_001350671.1:n.1005+127T>C
|
|
|
XM_005246084.2:c.573+127T>C
|
XP_005246141.1:n.573+127T>C
|
|
|
XM_005246086.2:c.522+127T>C
|
XP_005246143.1:n.522+127T>C
|
|
|
XM_006712608.3:c.753+127T>C
|
XP_006712671.1:n.753+127T>C
|
|
|
XR_001738801.2:n.1135+127T>C
|
|
|
|
XR_241242.3:n.1186+127T>C
|
|
|
|
NM_030803.7:c.954+127T>C
MANE Select
|
NP_110430.5:n.954+127T>C
|
|
|
NM_001190266.2:c.702+127T>C
|
NP_001177195.1:n.702+127T>C
|
|
|
NM_001190267.2:c.606+127T>C
|
NP_001177196.1:n.606+127T>C
|
|
|
NM_001363742.2:c.1005+127T>C
|
NP_001350671.1:n.1005+127T>C
|
|
|
NM_017974.4:c.897+127T>C
|
NP_060444.3:n.897+127T>C
|
|
|
NM_198890.3:c.465+127T>C
|
NP_942593.2:n.465+127T>C
|
|
