ENST00000686218.1:c.719T>C
|
ENSP00000509288.1:p.Met240Thr
|
|
ENST00000691144.1:n.3099T>C
|
|
|
ENST00000691249.1:n.1708T>C
|
|
|
ENST00000442944.7:c.866T>C
|
ENSP00000392041.3:p.Met289Thr
|
|
ENST00000640813.1:c.*121T>C
|
ENSP00000491061.1:n.*121T>C
|
|
ENST00000648026.1:c.778T>C
|
ENSP00000498044.1:n.778T>C
|
|
ENST00000648374.1:c.833T>C
|
ENSP00000497255.1:p.Met278Thr
|
|
ENST00000650101.1:c.815T>C
|
ENSP00000496970.1:p.Met272Thr
|
|
ENST00000650307.1:n.1710T>C
|
|
|
ENST00000652429.1:c.884T>C
MANE Select
|
ENSP00000498786.1:p.Met295Thr
|
|
ENST00000278715.7:c.884T>C
|
ENSP00000278715.3:p.Met295Thr
|
|
ENST00000392841.1:c.833T>C
|
ENSP00000376584.1:p.Met278Thr
|
|
ENST00000442944.6:c.833T>C
|
ENSP00000392041.2:p.Met278Thr
|
|
ENST00000537841.5:c.833T>C
|
ENSP00000444730.1:p.Met278Thr
|
|
ENST00000539045.1:n.383T>C
|
|
|
ENST00000542044.5:n.1329T>C
|
|
|
ENST00000542729.5:c.713T>C
|
ENSP00000443058.1:p.Met238Thr
|
|
ENST00000543090.5:c.791T>C
|
ENSP00000445429.1:p.Met264Thr
|
|
ENST00000543543.5:n.1359T>C
|
|
|
ENST00000544182.1:n.1333T>C
|
|
|
ENST00000544387.5:c.764T>C
|
ENSP00000438424.1:p.Met255Thr
|
|
ENST00000546226.5:n.1646T>C
|
|
|
NM_000190.3:c.884T>C
|
NP_000181.2:p.Met295Thr
|
|
NM_001024382.1:c.833T>C
|
NP_001019553.1:p.Met278Thr
|
|
NM_001258208.1:c.764T>C
|
NP_001245137.1:p.Met255Thr
|
|
NM_001258209.1:c.713T>C
|
NP_001245138.1:p.Met238Thr
|
|
XM_005271531.1:c.833T>C
|
XP_005271588.1:p.Met278Thr
|
|
XM_005271532.1:c.833T>C
|
XP_005271589.1:p.Met278Thr
|
|
XM_005271533.2:c.830T>C
|
XP_005271590.1:p.Met277Thr
|
|
XM_011542796.1:c.719T>C
|
XP_011541098.1:p.Met240Thr
|
|
NM_000190.4:c.884T>C
MANE Select
|
NP_000181.2:p.Met295Thr
|
|
NM_001024382.2:c.833T>C
|
NP_001019553.1:p.Met278Thr
|
|
XM_005271533.3:c.830T>C
|
XP_005271590.1:p.Met277Thr
|
|
XM_017017629.1:c.833T>C
|
XP_016873118.1:p.Met278Thr
|
|
XM_024448460.1:c.710T>C
|
XP_024304228.1:p.Met237Thr
|
|
NM_001258208.2:c.764T>C
|
NP_001245137.1:p.Met255Thr
|
|
NM_001258209.2:c.713T>C
|
NP_001245138.1:p.Met238Thr
|
|