|
NM_000069.3:c.4610T>C
MANE Select
|
NP_000060.2:p.Met1537Thr
|
|
ENST00000362061.4:c.4610T>C
MANE Select
|
ENSP00000355192.3:p.Met1537Thr
|
|
NM_000069.2:c.4610T>C
|
NP_000060.2:p.Met1537Thr
|
|
ENST00000362061.3:c.4610T>C
|
ENSP00000355192.3:p.Met1537Thr
|
|
ENST00000367338.7:c.4553T>C
|
ENSP00000356307.3:p.Met1518Thr
|
|
ENST00000679417.1:c.*3773T>C
|
ENSP00000506706.1:n.*3773T>C
|
|
ENST00000680051.1:n.1736T>C
|
|
|
ENST00000680059.1:c.*2128T>C
|
ENSP00000504944.1:n.*2128T>C
|
|
ENST00000681078.1:c.*385T>C
|
ENSP00000506645.1:n.*385T>C
|
|
ENST00000681190.1:c.*792T>C
|
ENSP00000506428.1:n.*792T>C
|
|
ENST00000681874.1:c.4550T>C
|
ENSP00000505162.1:p.Met1517Thr
|
|
XM_005245478.2:c.4553T>C
|
XP_005245535.1:p.Met1518Thr
|
|
XM_005245478.3:c.4553T>C
|
XP_005245535.1:p.Met1518Thr
|