ENST00000328300.11:c.4221A>G
MANE Select
|
ENSP00000331902.7:p.Pro1407=
|
|
ENST00000361603.7:c.4203A>G
|
ENSP00000354505.2:p.Pro1401=
|
|
ENST00000510690.2:n.715A>G
|
|
|
ENST00000328300.10:c.4221A>G
|
ENSP00000331902.6:p.Pro1407=
|
|
ENST00000361603.6:c.4203A>G
|
ENSP00000354505.2:p.Pro1401=
|
|
ENST00000489230.1:n.624A>G
|
|
|
ENST00000515658.1:c.17A>G
|
|
|
NM_000495.4:c.4203A>G
|
NP_000486.1:p.Pro1401=
|
|
NM_033380.2:c.4221A>G
|
NP_203699.1:p.Pro1407=
|
|
XM_005262070.2:c.4212A>G
|
XP_005262127.1:p.Pro1404=
|
|
XM_006724616.2:c.4221A>G
|
XP_006724679.1:p.Pro1407=
|
|
XM_011530849.1:c.3897A>G
|
XP_011529151.1:p.Pro1299=
|
|
XM_011530851.1:c.1794A>G
|
XP_011529153.1:p.Pro598=
|
|
XM_011530849.2:c.4236A>G
|
XP_011529151.2:p.Pro1412=
|
|
XM_017029259.2:c.4227A>G
|
XP_016884748.1:p.Pro1409=
|
|
XM_017029260.1:c.4218A>G
|
XP_016884749.1:p.Pro1406=
|
|
XM_017029263.2:c.2556A>G
|
XP_016884752.1:p.Pro852=
|
|
NM_000495.5:c.4203A>G
|
NP_000486.1:p.Pro1401=
|
|
NM_033380.3:c.4221A>G
MANE Select
|
NP_203699.1:p.Pro1407=
|
|