ENST00000328300.11:c.4055C>A
MANE Select
|
ENSP00000331902.7:p.Pro1352His
|
|
ENST00000361603.7:c.4037C>A
|
ENSP00000354505.2:p.Pro1346His
|
|
ENST00000510690.2:n.549C>A
|
|
|
ENST00000328300.10:c.4055C>A
|
ENSP00000331902.6:p.Pro1352His
|
|
ENST00000361603.6:c.4037C>A
|
ENSP00000354505.2:p.Pro1346His
|
|
ENST00000489230.1:n.458C>A
|
|
|
NM_000495.4:c.4037C>A
|
NP_000486.1:p.Pro1346His
|
|
NM_033380.2:c.4055C>A
|
NP_203699.1:p.Pro1352His
|
|
XM_005262070.2:c.4046C>A
|
XP_005262127.1:p.Pro1349His
|
|
XM_006724616.2:c.4055C>A
|
XP_006724679.1:p.Pro1352His
|
|
XM_011530849.1:c.3731C>A
|
XP_011529151.1:p.Pro1244His
|
|
XM_011530851.1:c.1628C>A
|
XP_011529153.1:p.Pro543His
|
|
XM_011530849.2:c.4070C>A
|
XP_011529151.2:p.Pro1357His
|
|
XM_017029259.2:c.4061C>A
|
XP_016884748.1:p.Pro1354His
|
|
XM_017029260.1:c.4052C>A
|
XP_016884749.1:p.Pro1351His
|
|
XM_017029263.2:c.2390C>A
|
XP_016884752.1:p.Pro797His
|
|
NM_000495.5:c.4037C>A
|
NP_000486.1:p.Pro1346His
|
|
NM_033380.3:c.4055C>A
MANE Select
|
NP_203699.1:p.Pro1352His
|
|