ENST00000328300.11:c.4779T>A
MANE Select
|
ENSP00000331902.7:p.Pro1593=
|
|
ENST00000361603.7:c.4761T>A
|
ENSP00000354505.2:p.Pro1587=
|
|
ENST00000510690.2:n.1273T>A
|
|
|
ENST00000644079.1:n.1265T>A
|
|
|
ENST00000328300.10:c.4779T>A
|
ENSP00000331902.6:p.Pro1593=
|
|
ENST00000361603.6:c.4761T>A
|
ENSP00000354505.2:p.Pro1587=
|
|
ENST00000504541.1:c.177T>A
|
ENSP00000424845.1:p.Pro59=
|
|
ENST00000515658.1:c.325-1418T>A
|
|
|
NM_000495.4:c.4761T>A
|
NP_000486.1:p.Pro1587=
|
|
NM_033380.2:c.4779T>A
|
NP_203699.1:p.Pro1593=
|
|
XM_005262070.2:c.4770T>A
|
XP_005262127.1:p.Pro1590=
|
|
XM_006724616.2:c.4779T>A
|
XP_006724679.1:p.Pro1593=
|
|
XM_011530849.1:c.4455T>A
|
XP_011529151.1:p.Pro1485=
|
|
XM_011530851.1:c.2352T>A
|
XP_011529153.1:p.Pro784=
|
|
XM_011530849.2:c.4794T>A
|
XP_011529151.2:p.Pro1598=
|
|
XM_017029259.2:c.4785T>A
|
XP_016884748.1:p.Pro1595=
|
|
XM_017029260.1:c.4776T>A
|
XP_016884749.1:p.Pro1592=
|
|
XM_017029263.2:c.3114T>A
|
XP_016884752.1:p.Pro1038=
|
|
NM_000495.5:c.4761T>A
|
NP_000486.1:p.Pro1587=
|
|
NM_033380.3:c.4779T>A
MANE Select
|
NP_203699.1:p.Pro1593=
|
|