ENST00000393655.4:c.81+152G>T
MANE Select
|
ENSP00000377265.2:n.81+152G>T
|
|
ENST00000344788.7:c.48+152G>T
|
ENSP00000342252.3:n.48+152G>T
|
|
ENST00000393655.3:c.81+152G>T
|
ENSP00000377265.2:n.81+152G>T
|
|
NM_003221.3:c.81+152G>T
|
NP_003212.2:n.81+152G>T
|
|
XM_006715176.2:c.81+152G>T
|
XP_006715239.1:n.81+152G>T
|
|
XM_011514834.1:c.81+152G>T
|
XP_011513136.1:n.81+152G>T
|
|
XM_011514835.1:c.81+152G>T
|
XP_011513137.1:n.81+152G>T
|
|
XM_011514836.1:c.81+152G>T
|
XP_011513138.1:n.81+152G>T
|
|
XM_011514837.1:c.81+152G>T
|
XP_011513139.1:n.81+152G>T
|
|
XM_011514837.2:c.81+152G>T
|
XP_011513139.1:n.81+152G>T
|
|
XM_017011233.1:c.173+152G>T
|
XP_016866722.1:n.173+152G>T
|
|
XM_017011234.1:c.137+152G>T
|
XP_016866723.1:n.137+152G>T
|
|
XM_017011235.2:c.81+152G>T
|
XP_016866724.1:n.81+152G>T
|
|
NM_003221.4:c.81+152G>T
MANE Select
|
NP_003212.2:n.81+152G>T
|
|