ENST00000650516.2:c.1797-86G=
|
ENSP00000498052.2:n.1797-86G=
|
|
ENST00000343257.7:c.1797-86G=
MANE Select
|
ENSP00000339867.2:n.1797-86G=
|
|
ENST00000432192.6:c.1621-86G=
|
|
|
ENST00000343257.6:c.1797-86G=
|
ENSP00000339867.2:n.1797-86G=
|
|
NM_000083.2:c.1797-86G=
|
NP_000074.2:n.1797-86G=
|
|
NR_046453.1:n.1737-86G=
|
|
|
XM_011515781.1:c.1821-86G=
|
XP_011514083.1:n.1821-86G=
|
|
XM_011515782.1:c.543-86G=
|
XP_011514084.1:n.543-86G=
|
|
XM_011515782.2:c.543-86G=
|
XP_011514084.1:n.543-86G=
|
|
XM_017011739.1:c.1371-86G=
|
XP_016867228.1:n.1371-86G=
|
|
XM_017011740.1:c.1347-86G=
|
XP_016867229.1:n.1347-86G=
|
|
NM_000083.3:c.1797-86G=
MANE Select
|
NP_000074.3:n.1797-86G=
|
|
NR_046453.2:n.1752-86G=
|
|
|