ENST00000328300.11:c.4438C>G
MANE Select
|
ENSP00000331902.7:p.Pro1480Ala
|
|
ENST00000361603.7:c.4420C>G
|
ENSP00000354505.2:p.Pro1474Ala
|
|
ENST00000510690.2:n.932C>G
|
|
|
ENST00000328300.10:c.4438C>G
|
ENSP00000331902.6:p.Pro1480Ala
|
|
ENST00000361603.6:c.4420C>G
|
ENSP00000354505.2:p.Pro1474Ala
|
|
ENST00000515658.1:c.234C>G
|
|
|
NM_000495.4:c.4420C>G
|
NP_000486.1:p.Pro1474Ala
|
|
NM_033380.2:c.4438C>G
|
NP_203699.1:p.Pro1480Ala
|
|
XM_005262070.2:c.4429C>G
|
XP_005262127.1:p.Pro1477Ala
|
|
XM_006724616.2:c.4438C>G
|
XP_006724679.1:p.Pro1480Ala
|
|
XM_011530849.1:c.4114C>G
|
XP_011529151.1:p.Pro1372Ala
|
|
XM_011530851.1:c.2011C>G
|
XP_011529153.1:p.Pro671Ala
|
|
XM_011530849.2:c.4453C>G
|
XP_011529151.2:p.Pro1485Ala
|
|
XM_017029259.2:c.4444C>G
|
XP_016884748.1:p.Pro1482Ala
|
|
XM_017029260.1:c.4435C>G
|
XP_016884749.1:p.Pro1479Ala
|
|
XM_017029263.2:c.2773C>G
|
XP_016884752.1:p.Pro925Ala
|
|
NM_000495.5:c.4420C>G
|
NP_000486.1:p.Pro1474Ala
|
|
NM_033380.3:c.4438C>G
MANE Select
|
NP_203699.1:p.Pro1480Ala
|
|