ENST00000442488.7:c.801+59C>T
MANE Select
|
ENSP00000411145.2:n.801+59C>T
|
|
ENST00000427185.2:c.651+59C>T
|
ENSP00000392727.2:n.651+59C>T
|
|
ENST00000442488.6:c.801+59C>T
|
ENSP00000411145.2:n.801+59C>T
|
|
NM_001024613.3:c.801+59C>T
|
NP_001019784.2:n.801+59C>T
|
|
NM_001160264.2:c.651+59C>T
|
NP_001153736.1:n.651+59C>T
|
|
XM_005250337.2:c.801+59C>T
|
XP_005250394.1:n.801+59C>T
|
|
XM_011516200.1:c.801+59C>T
|
XP_011514502.1:n.801+59C>T
|
|
XM_011516201.1:c.801+59C>T
|
XP_011514503.1:n.801+59C>T
|
|
XM_011516202.1:c.651+59C>T
|
XP_011514504.1:n.651+59C>T
|
|
XM_005250337.3:c.801+59C>T
|
XP_005250394.1:n.801+59C>T
|
|
XM_011516202.2:c.651+59C>T
|
XP_011514504.1:n.651+59C>T
|
|
NM_001024613.4:c.801+59C>T
MANE Select
|
NP_001019784.2:n.801+59C>T
|
|