ENST00000328300.11:c.4258C>T
MANE Select
|
ENSP00000331902.7:p.Pro1420Ser
|
|
ENST00000361603.7:c.4240C>T
|
ENSP00000354505.2:p.Pro1414Ser
|
|
ENST00000510690.2:n.752C>T
|
|
|
ENST00000328300.10:c.4258C>T
|
ENSP00000331902.6:p.Pro1420Ser
|
|
ENST00000361603.6:c.4240C>T
|
ENSP00000354505.2:p.Pro1414Ser
|
|
ENST00000489230.1:n.661C>T
|
|
|
ENST00000515658.1:c.54C>T
|
|
|
NM_000495.4:c.4240C>T
|
NP_000486.1:p.Pro1414Ser
|
|
NM_033380.2:c.4258C>T
|
NP_203699.1:p.Pro1420Ser
|
|
XM_005262070.2:c.4249C>T
|
XP_005262127.1:p.Pro1417Ser
|
|
XM_006724616.2:c.4258C>T
|
XP_006724679.1:p.Pro1420Ser
|
|
XM_011530849.1:c.3934C>T
|
XP_011529151.1:p.Pro1312Ser
|
|
XM_011530851.1:c.1831C>T
|
XP_011529153.1:p.Pro611Ser
|
|
XM_011530849.2:c.4273C>T
|
XP_011529151.2:p.Pro1425Ser
|
|
XM_017029259.2:c.4264C>T
|
XP_016884748.1:p.Pro1422Ser
|
|
XM_017029260.1:c.4255C>T
|
XP_016884749.1:p.Pro1419Ser
|
|
XM_017029263.2:c.2593C>T
|
XP_016884752.1:p.Pro865Ser
|
|
NM_000495.5:c.4240C>T
|
NP_000486.1:p.Pro1414Ser
|
|
NM_033380.3:c.4258C>T
MANE Select
|
NP_203699.1:p.Pro1420Ser
|
|