|
NM_007083.5:c.498+6943A>G
MANE Select
|
NP_009014.2:n.498+6943A>G
|
|
ENST00000304430.10:c.498+6943A>G
MANE Select
|
ENSP00000306070.5:n.498+6943A>G
|
|
NM_007083.4:c.498+6943A>G
|
NP_009014.2:n.498+6943A>G
|
|
NM_198041.2:c.-10+6943A>G
|
NP_932158.1:n.-10+6943A>G
|
|
NM_198041.3:c.-10+6943A>G
|
NP_932158.1:n.-10+6943A>G
|
|
ENST00000304430.9:c.498+6943A>G
|
ENSP00000306070.5:n.498+6943A>G
|
|
ENST00000339154.6:c.-10+6943A>G
|
ENSP00000344011.2:n.-10+6943A>G
|
|
ENST00000502270.5:c.-10+6943A>G
|
ENSP00000424117.1:n.-10+6943A>G
|
|
ENST00000503370.5:c.*494+6943A>G
|
ENSP00000422698.1:n.*494+6943A>G
|
|
ENST00000510735.1:c.109-7947A>G
|
|
|
ENST00000512116.5:c.*589+6943A>G
|
ENSP00000420843.1:n.*589+6943A>G
|
|
ENST00000513517.1:n.5153+6943A>G
|
|