ENST00000278353.10:c.160+25547C>G
MANE Select
|
ENSP00000278353.4:n.160+25547C>G
|
|
ENST00000527433.6:c.123+25730C>G
|
ENSP00000490749.1:n.123+25730C>G
|
|
ENST00000636007.1:c.160+25547C>G
|
ENSP00000490822.1:n.160+25547C>G
|
|
ENST00000636722.1:c.*20+25351C>G
|
ENSP00000490003.1:n.*20+25351C>G
|
|
ENST00000637401.1:c.160+25547C>G
|
ENSP00000490421.1:n.160+25547C>G
|
|
ENST00000638034.1:c.64+25177C>G
|
ENSP00000490701.1:n.64+25177C>G
|
|
ENST00000278353.8:c.160+25547C>G
|
ENSP00000278353.4:n.160+25547C>G
|
|
ENST00000395700.4:c.160+25547C>G
|
ENSP00000379052.4:n.160+25547C>G
|
|
ENST00000527433.5:n.125+25730C>G
|
|
|
ENST00000529261.5:n.377+33395C>G
|
|
|
ENST00000531185.5:c.160+25547C>G
|
ENSP00000436582.1:n.160+25547C>G
|
|
ENST00000532864.5:n.282-44377C>G
|
|
|
NM_016142.2:c.160+25547C>G
|
NP_057226.1:n.160+25547C>G
|
|
XM_011520156.1:c.-63+25351C>G
|
XP_011518458.1:n.-63+25351C>G
|
|
XM_017017881.1:c.64+25177C>G
|
XP_016873370.1:n.64+25177C>G
|
|
XM_024448571.1:c.-62-44377C>G
|
XP_024304339.1:n.-62-44377C>G
|
|
XM_024448572.1:c.-62-44377C>G
|
XP_024304340.1:n.-62-44377C>G
|
|
XM_024448573.1:c.-62-44377C>G
|
XP_024304341.1:n.-62-44377C>G
|
|
NM_016142.3:c.160+25547C>G
MANE Select
|
NP_057226.1:n.160+25547C>G
|
|