ENST00000328300.11:c.4339C>A
MANE Select
|
ENSP00000331902.7:p.Pro1447Thr
|
|
ENST00000361603.7:c.4321C>A
|
ENSP00000354505.2:p.Pro1441Thr
|
|
ENST00000510690.2:n.833C>A
|
|
|
ENST00000328300.10:c.4339C>A
|
ENSP00000331902.6:p.Pro1447Thr
|
|
ENST00000361603.6:c.4321C>A
|
ENSP00000354505.2:p.Pro1441Thr
|
|
ENST00000515658.1:c.135C>A
|
|
|
NM_000495.4:c.4321C>A
|
NP_000486.1:p.Pro1441Thr
|
|
NM_033380.2:c.4339C>A
|
NP_203699.1:p.Pro1447Thr
|
|
XM_005262070.2:c.4330C>A
|
XP_005262127.1:p.Pro1444Thr
|
|
XM_006724616.2:c.4339C>A
|
XP_006724679.1:p.Pro1447Thr
|
|
XM_011530849.1:c.4015C>A
|
XP_011529151.1:p.Pro1339Thr
|
|
XM_011530851.1:c.1912C>A
|
XP_011529153.1:p.Pro638Thr
|
|
XM_011530849.2:c.4354C>A
|
XP_011529151.2:p.Pro1452Thr
|
|
XM_017029259.2:c.4345C>A
|
XP_016884748.1:p.Pro1449Thr
|
|
XM_017029260.1:c.4336C>A
|
XP_016884749.1:p.Pro1446Thr
|
|
XM_017029263.2:c.2674C>A
|
XP_016884752.1:p.Pro892Thr
|
|
NM_000495.5:c.4321C>A
|
NP_000486.1:p.Pro1441Thr
|
|
NM_033380.3:c.4339C>A
MANE Select
|
NP_203699.1:p.Pro1447Thr
|
|