|
ENST00000287387.7:c.508+776C>T
MANE Select
|
ENSP00000287387.2:n.508+776C>T
|
|
|
ENST00000650311.1:c.328+776C>T
|
ENSP00000497747.1:n.328+776C>T
|
|
|
ENST00000287387.6:c.508+776C>T
|
ENSP00000287387.2:n.508+776C>T
|
|
|
ENST00000517609.5:n.591+776C>T
|
|
|
|
ENST00000518125.1:c.64+776C>T
|
ENSP00000429258.1:n.64+776C>T
|
|
|
ENST00000519199.5:c.658+776C>T
|
|
|
|
ENST00000523356.1:c.509-24C>T
|
ENSP00000428615.1:n.509-24C>T
|
|
|
ENST00000523551.1:n.479+776C>T
|
|
|
|
ENST00000523984.5:c.328+776C>T
|
ENSP00000430427.1:n.328+776C>T
|
|
|
ENST00000524254.5:n.527+776C>T
|
|
|
|
NM_001283024.1:c.328+776C>T
|
NP_001269953.1:n.328+776C>T
|
|
|
NM_001283027.1:c.304+776C>T
|
NP_001269956.1:n.304+776C>T
|
|
|
NM_018024.2:c.508+776C>T
|
NP_060494.1:n.508+776C>T
|
|
|
XM_006716597.2:c.509-24C>T
|
XP_006716660.1:n.509-24C>T
|
|
|
XM_011517146.1:c.508+776C>T
|
XP_011515448.1:n.508+776C>T
|
|
|
XM_011517147.1:c.508+776C>T
|
XP_011515449.1:n.508+776C>T
|
|
|
XM_011517148.1:c.328+776C>T
|
XP_011515450.1:n.328+776C>T
|
|
|
XM_011517149.1:c.304+776C>T
|
XP_011515451.1:n.304+776C>T
|
|
|
XM_011517150.1:c.304+776C>T
|
XP_011515452.1:n.304+776C>T
|
|
|
XM_011517151.1:c.304+776C>T
|
XP_011515453.1:n.304+776C>T
|
|
|
XR_928337.1:n.633+776C>T
|
|
|
|
XR_928338.1:n.546+776C>T
|
|
|
|
NR_133926.1:n.557+776C>T
|
|
|
|
XM_006716597.3:c.509-24C>T
|
XP_006716660.1:n.509-24C>T
|
|
|
XM_011517151.2:c.304+776C>T
|
XP_011515453.1:n.304+776C>T
|
|
|
XM_017013601.1:c.508+776C>T
|
XP_016869090.1:n.508+776C>T
|
|
|
XM_017013602.1:c.328+776C>T
|
XP_016869091.1:n.328+776C>T
|
|
|
XM_017013603.1:c.328+776C>T
|
XP_016869092.1:n.328+776C>T
|
|
|
XR_002956634.1:n.626+776C>T
|
|
|
|
XR_002956635.1:n.581+776C>T
|
|
|
|
XR_002956636.1:n.581+776C>T
|
|
|
|
XR_928337.3:n.633+776C>T
|
|
|
|
NM_018024.3:c.508+776C>T
MANE Select
|
NP_060494.1:n.508+776C>T
|
|
|
NR_133926.2:n.508+776C>T
|
|
|
