ENST00000328300.11:c.4086A>T
MANE Select
|
ENSP00000331902.7:p.Pro1362=
|
|
ENST00000361603.7:c.4068A>T
|
ENSP00000354505.2:p.Pro1356=
|
|
ENST00000510690.2:n.580A>T
|
|
|
ENST00000328300.10:c.4086A>T
|
ENSP00000331902.6:p.Pro1362=
|
|
ENST00000361603.6:c.4068A>T
|
ENSP00000354505.2:p.Pro1356=
|
|
ENST00000489230.1:n.489A>T
|
|
|
NM_000495.4:c.4068A>T
|
NP_000486.1:p.Pro1356=
|
|
NM_033380.2:c.4086A>T
|
NP_203699.1:p.Pro1362=
|
|
XM_005262070.2:c.4077A>T
|
XP_005262127.1:p.Pro1359=
|
|
XM_006724616.2:c.4086A>T
|
XP_006724679.1:p.Pro1362=
|
|
XM_011530849.1:c.3762A>T
|
XP_011529151.1:p.Pro1254=
|
|
XM_011530851.1:c.1659A>T
|
XP_011529153.1:p.Pro553=
|
|
XM_011530849.2:c.4101A>T
|
XP_011529151.2:p.Pro1367=
|
|
XM_017029259.2:c.4092A>T
|
XP_016884748.1:p.Pro1364=
|
|
XM_017029260.1:c.4083A>T
|
XP_016884749.1:p.Pro1361=
|
|
XM_017029263.2:c.2421A>T
|
XP_016884752.1:p.Pro807=
|
|
NM_000495.5:c.4068A>T
|
NP_000486.1:p.Pro1356=
|
|
NM_033380.3:c.4086A>T
MANE Select
|
NP_203699.1:p.Pro1362=
|
|