ENST00000328300.11:c.4216+60G>T
MANE Select
|
ENSP00000331902.7:n.4216+60G>T
|
|
ENST00000361603.7:c.4198+60G>T
|
ENSP00000354505.2:n.4198+60G>T
|
|
ENST00000510690.2:n.710+60G>T
|
|
|
ENST00000328300.10:c.4216+60G>T
|
ENSP00000331902.6:n.4216+60G>T
|
|
ENST00000361603.6:c.4198+60G>T
|
ENSP00000354505.2:n.4198+60G>T
|
|
ENST00000489230.1:n.619+60G>T
|
|
|
ENST00000515658.1:c.12+60G>T
|
|
|
NM_000495.4:c.4198+60G>T
|
NP_000486.1:n.4198+60G>T
|
|
NM_033380.2:c.4216+60G>T
|
NP_203699.1:n.4216+60G>T
|
|
XM_005262070.2:c.4207+60G>T
|
XP_005262127.1:n.4207+60G>T
|
|
XM_006724616.2:c.4216+60G>T
|
XP_006724679.1:n.4216+60G>T
|
|
XM_011530849.1:c.3892+60G>T
|
XP_011529151.1:n.3892+60G>T
|
|
XM_011530851.1:c.1789+60G>T
|
XP_011529153.1:n.1789+60G>T
|
|
XM_011530849.2:c.4231+60G>T
|
XP_011529151.2:n.4231+60G>T
|
|
XM_017029259.2:c.4222+60G>T
|
XP_016884748.1:n.4222+60G>T
|
|
XM_017029260.1:c.4213+60G>T
|
XP_016884749.1:n.4213+60G>T
|
|
XM_017029263.2:c.2551+60G>T
|
XP_016884752.1:n.2551+60G>T
|
|
NM_000495.5:c.4198+60G>T
|
NP_000486.1:n.4198+60G>T
|
|
NM_033380.3:c.4216+60G>T
MANE Select
|
NP_203699.1:n.4216+60G>T
|
|