ENST00000355699.7:c.3057G>A
MANE Select
|
ENSP00000347927.2:p.Met1019Ile
|
|
ENST00000355699.6:c.3057G>A
|
ENSP00000347927.2:p.Met1019Ile
|
|
ENST00000356589.6:c.2964G>A
|
ENSP00000348997.2:p.Met988Ile
|
|
ENST00000371916.5:c.*526G>A
|
ENSP00000360984.2:n.*526G>A
|
|
ENST00000371929.7:c.3057G>A
|
ENSP00000360997.3:p.Met1019Ile
|
|
ENST00000485925.5:n.1873G>A
|
|
|
NM_139025.4:c.3057G>A , LRG_544t1:c.3057G>A
|
NP_620594.1:p.Met1019Ile
|
|
NM_139026.4:c.2964G>A
|
NP_620595.1:p.Met988Ile
|
|
NM_139027.4:c.3057G>A
|
NP_620596.2:p.Met1019Ile
|
|
NR_024514.2:n.1892G>A
|
|
|
XM_011518174.1:c.2667G>A
|
XP_011516476.1:p.Met889Ile
|
|
XM_011518175.1:c.3057G>A
|
XP_011516477.1:p.Met1019Ile
|
|
XM_011518176.1:c.2073G>A
|
XP_011516478.1:p.Met691Ile
|
|
XM_011518177.1:c.2067G>A
|
XP_011516479.1:p.Met689Ile
|
|
XM_011518178.1:c.1722G>A
|
XP_011516480.1:p.Met574Ile
|
|
XM_011518179.1:c.1722G>A
|
XP_011516481.1:p.Met574Ile
|
|
XM_011518180.1:c.1323G>A
|
XP_011516482.1:p.Met441Ile
|
|
XM_011518176.3:c.2073G>A
|
XP_011516478.1:p.Met691Ile
|
|
XM_011518178.2:c.1722G>A
|
XP_011516480.1:p.Met574Ile
|
|
XM_017014232.1:c.3045G>A
|
XP_016869721.1:p.Met1015Ile
|
|
XM_017014233.1:c.2667G>A
|
XP_016869722.1:p.Met889Ile
|
|
XM_017014234.2:c.2067G>A
|
XP_016869723.1:p.Met689Ile
|
|
XR_001746171.1:n.3830G>A
|
|
|
NM_139026.5:c.2964G>A
|
NP_620595.1:p.Met988Ile
|
|
NM_139027.5:c.3057G>A
|
NP_620596.2:p.Met1019Ile
|
|
NM_139025.5:c.3057G>A
|
NP_620594.1:p.Met1019Ile
|
|
NM_139026.6:c.2964G>A
|
NP_620595.1:p.Met988Ile
|
|
NM_139027.6:c.3057G>A
MANE Select
|
NP_620596.2:p.Met1019Ile
|
|
NR_024514.3:n.1894G>A
|
|
|