|
ENST00000261937.11:c.3807+121C>T
MANE Select
|
ENSP00000261937.6:n.3807+121C>T
|
|
|
ENST00000261937.10:c.3807+121C>T
|
ENSP00000261937.6:n.3807+121C>T
|
|
|
ENST00000393347.7:c.3807+121C>T
|
ENSP00000377016.3:n.3807+121C>T
|
|
|
ENST00000502603.5:n.507+121C>T
|
|
|
|
ENST00000502649.5:c.3807+121C>T
|
ENSP00000426057.1:n.3807+121C>T
|
|
|
ENST00000507059.5:n.4278C>T
|
|
|
|
ENST00000619105.4:c.*2750+121C>T
|
ENSP00000481134.1:n.*2750+121C>T
|
|
|
NM_002020.4:c.3807+121C>T
|
NP_002011.2:n.3807+121C>T
|
|
|
NM_182925.4:c.3807+121C>T
|
NP_891555.2:n.3807+121C>T
|
|
|
XM_011534477.1:c.4056+121C>T
|
XP_011532779.1:n.4056+121C>T
|
|
|
XM_011534478.1:c.4038+121C>T
|
XP_011532780.1:n.4038+121C>T
|
|
|
XM_011534479.1:c.4056+121C>T
|
XP_011532781.1:n.4056+121C>T
|
|
|
XM_011534480.1:c.4056+121C>T
|
XP_011532782.1:n.4056+121C>T
|
|
|
XM_011534481.1:c.4056+121C>T
|
XP_011532783.1:n.4056+121C>T
|
|
|
XM_011534482.1:c.3825+121C>T
|
XP_011532784.1:n.3825+121C>T
|
|
|
XM_011534483.1:c.3747+121C>T
|
XP_011532785.1:n.3747+121C>T
|
|
|
XM_011534484.1:c.3348+121C>T
|
XP_011532786.1:n.3348+121C>T
|
|
|
XR_941095.1:n.4093+121C>T
|
|
|
|
NM_001354989.1:c.3807+121C>T
|
NP_001341918.1:n.3807+121C>T
|
|
|
XM_011534478.3:c.4038+121C>T
|
XP_011532780.1:n.4038+121C>T
|
|
|
XM_011534484.2:c.3348+121C>T
|
XP_011532786.1:n.3348+121C>T
|
|
|
XM_017009263.1:c.4038+121C>T
|
XP_016864752.1:n.4038+121C>T
|
|
|
XM_017009264.2:c.4038+121C>T
|
XP_016864753.1:n.4038+121C>T
|
|
|
XM_017009265.1:c.4038+121C>T
|
XP_016864754.1:n.4038+121C>T
|
|
|
XM_017009266.1:c.4038+121C>T
|
XP_016864755.1:n.4038+121C>T
|
|
|
XM_017009267.2:c.4038+121C>T
|
XP_016864756.1:n.4038+121C>T
|
|
|
XM_017009268.1:c.3729+121C>T
|
XP_016864757.1:n.3729+121C>T
|
|
|
XR_001742050.2:n.4297+121C>T
|
|
|
|
NM_182925.5:c.3807+121C>T
MANE Select
|
NP_891555.2:n.3807+121C>T
|
|
|
NM_001354989.2:c.3807+121C>T
|
NP_001341918.1:n.3807+121C>T
|
|
|
NM_002020.5:c.3807+121C>T
|
NP_002011.2:n.3807+121C>T
|
|
