ENST00000366577.10:c.1826T>C
MANE Select
|
ENSP00000355536.5:p.Met609Thr
|
|
ENST00000535889.6:c.1826T>C
|
ENSP00000441845.1:p.Met609Thr
|
|
ENST00000650888.1:c.*868T>C
|
ENSP00000498393.1:n.*868T>C
|
|
ENST00000651455.1:c.*570T>C
|
ENSP00000498963.1:n.*570T>C
|
|
ENST00000674797.2:c.1478T>C
|
ENSP00000502299.2:p.Met493Thr
|
|
ENST00000679569.1:n.2140T>C
|
|
|
ENST00000679842.1:c.1826T>C
|
ENSP00000506109.1:p.Met609Thr
|
|
ENST00000680454.1:n.2270T>C
|
|
|
ENST00000681102.1:c.1646T>C
|
ENSP00000505600.1:p.Met549Thr
|
|
ENST00000681177.1:c.1516-6872T>C
|
ENSP00000506327.1:n.1516-6872T>C
|
|
ENST00000681937.1:n.2148-6872T>C
|
|
|
ENST00000366576.3:c.488T>C
|
ENSP00000355535.3:p.Met163Thr
|
|
ENST00000366577.9:c.1826T>C
|
ENSP00000355536.5:p.Met609Thr
|
|
ENST00000463959.1:n.1845T>C
|
|
|
ENST00000535889.5:c.1826T>C
|
ENSP00000441845.1:p.Met609Thr
|
|
NM_000254.2:c.1826T>C
|
NP_000245.2:p.Met609Thr
|
|
NM_001291939.1:c.1826T>C
|
NP_001278868.1:p.Met609Thr
|
|
NM_001291940.1:c.605T>C
|
NP_001278869.1:p.Met202Thr
|
|
XM_005273141.3:c.1823T>C
|
XP_005273198.1:p.Met608Thr
|
|
XM_006711769.2:c.1826T>C
|
XP_006711832.1:p.Met609Thr
|
|
XM_006711770.1:c.890T>C
|
XP_006711833.1:p.Met297Thr
|
|
XM_011544193.1:c.1826T>C
|
XP_011542495.1:p.Met609Thr
|
|
XM_011544194.1:c.1994T>C
|
XP_011542496.1:p.Met665Thr
|
|
XM_005273141.5:c.1823T>C
|
XP_005273198.1:p.Met608Thr
|
|
XM_006711770.3:c.890T>C
|
XP_006711833.1:p.Met297Thr
|
|
XM_011544194.3:c.1994T>C
|
XP_011542496.1:p.Met665Thr
|
|
XM_017001329.2:c.1994T>C
|
XP_016856818.1:p.Met665Thr
|
|
XM_017001330.2:c.1994T>C
|
XP_016856819.1:p.Met665Thr
|
|
NM_001291940.2:c.605T>C
|
NP_001278869.1:p.Met202Thr
|
|
NM_000254.3:c.1826T>C
MANE Select
|
NP_000245.2:p.Met609Thr
|
|