ENST00000309822.7:c.*272A>G
MANE Select
|
ENSP00000308332.2:n.*272A>G
|
|
ENST00000309822.6:c.*272A>G
|
ENSP00000308332.2:n.*272A>G
|
|
ENST00000517814.1:c.363+1748A>G
|
ENSP00000429962.1:n.363+1748A>G
|
|
ENST00000517820.1:c.188+5323A>G
|
ENSP00000427767.1:n.188+5323A>G
|
|
ENST00000520733.5:c.45+1748A>G
|
ENSP00000429384.1:n.45+1748A>G
|
|
ENST00000521071.1:c.188+5323A>G
|
ENSP00000430029.1:n.188+5323A>G
|
|
ENST00000521703.5:c.188+5323A>G
|
ENSP00000428455.1:n.188+5323A>G
|
|
ENST00000524128.1:c.45+1748A>G
|
ENSP00000430309.1:n.45+1748A>G
|
|
NM_032334.2:c.*272A>G
|
NP_115710.2:n.*272A>G
|
|
XM_005251080.2:c.363+1748A>G
|
XP_005251137.2:n.363+1748A>G
|
|
XR_928356.1:n.411+1748A>G
|
|
|
XR_928357.1:n.411+1748A>G
|
|
|
NM_032334.3:c.*272A>G
MANE Select
|
NP_115710.2:n.*272A>G
|
|