ENST00000684241.1:n.3392G>A
|
|
|
ENST00000262186.10:c.2559G>A
MANE Select
|
ENSP00000262186.5:p.Trp853Ter
|
|
ENST00000330883.9:c.1539G>A
|
ENSP00000328531.4:p.Trp513Ter
|
|
ENST00000262186.9:c.2559G>A
|
ENSP00000262186.5:p.Trp853Ter
|
|
ENST00000330883.8:c.1539G>A
|
ENSP00000328531.4:p.Trp513Ter
|
|
NM_000238.3:c.2559G>A , LRG_288t1:c.2559G>A
|
NP_000229.1:p.Trp853Ter
|
|
NM_172057.2:c.1539G>A , LRG_288t3:c.1539G>A
|
NP_742054.1:p.Trp513Ter
|
|
XM_011516185.1:c.2259G>A
|
XP_011514487.1:p.Trp753Ter
|
|
XM_011516186.1:c.2559G>A
|
XP_011514488.1:p.Trp853Ter
|
|
XM_011516185.2:c.2259G>A
|
XP_011514487.1:p.Trp753Ter
|
|
XM_011516186.3:c.2559G>A
|
XP_011514488.1:p.Trp853Ter
|
|
XM_017012195.1:c.2409G>A
|
XP_016867684.1:p.Trp803Ter
|
|
XM_017012196.1:c.2382G>A
|
XP_016867685.1:p.Trp794Ter
|
|
NM_000238.4:c.2559G>A
MANE Select
|
NP_000229.1:p.Trp853Ter
|
|
NM_172057.3:c.1539G>A
|
NP_742054.1:p.Trp513Ter
|
|