ENST00000328300.11:c.4901C>T
MANE Select
|
ENSP00000331902.7:p.Pro1634Leu
|
|
ENST00000361603.7:c.4883C>T
|
ENSP00000354505.2:p.Pro1628Leu
|
|
ENST00000510690.2:n.1395C>T
|
|
|
ENST00000644079.1:n.1732C>T
|
|
|
ENST00000328300.10:c.4901C>T
|
ENSP00000331902.6:p.Pro1634Leu
|
|
ENST00000361603.6:c.4883C>T
|
ENSP00000354505.2:p.Pro1628Leu
|
|
ENST00000504541.1:c.219+425C>T
|
ENSP00000424845.1:n.219+425C>T
|
|
ENST00000515658.1:c.325-951C>T
|
|
|
NM_000495.4:c.4883C>T
|
NP_000486.1:p.Pro1628Leu
|
|
NM_033380.2:c.4901C>T
|
NP_203699.1:p.Pro1634Leu
|
|
XM_005262070.2:c.4892C>T
|
XP_005262127.1:p.Pro1631Leu
|
|
XM_006724616.2:c.4901C>T
|
XP_006724679.1:p.Pro1634Leu
|
|
XM_011530849.1:c.4577C>T
|
XP_011529151.1:p.Pro1526Leu
|
|
XM_011530851.1:c.2474C>T
|
XP_011529153.1:p.Pro825Leu
|
|
XM_011530849.2:c.4916C>T
|
XP_011529151.2:p.Pro1639Leu
|
|
XM_017029259.2:c.4907C>T
|
XP_016884748.1:p.Pro1636Leu
|
|
XM_017029260.1:c.4898C>T
|
XP_016884749.1:p.Pro1633Leu
|
|
XM_017029263.2:c.3236C>T
|
XP_016884752.1:p.Pro1079Leu
|
|
NM_000495.5:c.4883C>T
|
NP_000486.1:p.Pro1628Leu
|
|
NM_033380.3:c.4901C>T
MANE Select
|
NP_203699.1:p.Pro1634Leu
|
|