ENST00000650516.2:c.1796+110T>C
|
ENSP00000498052.2:n.1796+110T>C
|
|
ENST00000343257.7:c.1796+110T>C
MANE Select
|
ENSP00000339867.2:n.1796+110T>C
|
|
ENST00000432192.6:c.1620+110T>C
|
|
|
ENST00000343257.6:c.1796+110T>C
|
ENSP00000339867.2:n.1796+110T>C
|
|
NM_000083.2:c.1796+110T>C
|
NP_000074.2:n.1796+110T>C
|
|
NR_046453.1:n.1736+110T>C
|
|
|
XM_011515781.1:c.1820+110T>C
|
XP_011514083.1:n.1820+110T>C
|
|
XM_011515782.1:c.542+110T>C
|
XP_011514084.1:n.542+110T>C
|
|
XM_011515782.2:c.542+110T>C
|
XP_011514084.1:n.542+110T>C
|
|
XM_017011739.1:c.1370+110T>C
|
XP_016867228.1:n.1370+110T>C
|
|
XM_017011740.1:c.1346+110T>C
|
XP_016867229.1:n.1346+110T>C
|
|
NM_000083.3:c.1796+110T>C
MANE Select
|
NP_000074.3:n.1796+110T>C
|
|
NR_046453.2:n.1751+110T>C
|
|
|