ENST00000328300.11:c.4102C>A
MANE Select
|
ENSP00000331902.7:p.Pro1368Thr
|
|
ENST00000361603.7:c.4084C>A
|
ENSP00000354505.2:p.Pro1362Thr
|
|
ENST00000510690.2:n.596C>A
|
|
|
ENST00000328300.10:c.4102C>A
|
ENSP00000331902.6:p.Pro1368Thr
|
|
ENST00000361603.6:c.4084C>A
|
ENSP00000354505.2:p.Pro1362Thr
|
|
ENST00000489230.1:n.505C>A
|
|
|
NM_000495.4:c.4084C>A
|
NP_000486.1:p.Pro1362Thr
|
|
NM_033380.2:c.4102C>A
|
NP_203699.1:p.Pro1368Thr
|
|
XM_005262070.2:c.4093C>A
|
XP_005262127.1:p.Pro1365Thr
|
|
XM_006724616.2:c.4102C>A
|
XP_006724679.1:p.Pro1368Thr
|
|
XM_011530849.1:c.3778C>A
|
XP_011529151.1:p.Pro1260Thr
|
|
XM_011530851.1:c.1675C>A
|
XP_011529153.1:p.Pro559Thr
|
|
XM_011530849.2:c.4117C>A
|
XP_011529151.2:p.Pro1373Thr
|
|
XM_017029259.2:c.4108C>A
|
XP_016884748.1:p.Pro1370Thr
|
|
XM_017029260.1:c.4099C>A
|
XP_016884749.1:p.Pro1367Thr
|
|
XM_017029263.2:c.2437C>A
|
XP_016884752.1:p.Pro813Thr
|
|
NM_000495.5:c.4084C>A
|
NP_000486.1:p.Pro1362Thr
|
|
NM_033380.3:c.4102C>A
MANE Select
|
NP_203699.1:p.Pro1368Thr
|
|