ENST00000426508.7:c.4331T>C
MANE Select
|
ENSP00000406012.2:p.Met1444Thr
|
|
ENST00000361339.9:c.1913T>C
|
ENSP00000354895.5:p.Met638Thr
|
|
ENST00000397417.6:c.*2769T>C
|
ENSP00000380562.2:n.*2769T>C
|
|
ENST00000426508.6:c.4331T>C
|
ENSP00000406012.2:p.Met1444Thr
|
|
ENST00000565298.5:n.4155T>C
|
|
|
NM_014714.3:c.4331T>C
|
NP_055529.2:p.Met1444Thr
|
|
XM_006720989.2:c.4331T>C
|
XP_006721052.1:p.Met1444Thr
|
|
XM_006720990.2:c.4331T>C
|
XP_006721053.1:p.Met1444Thr
|
|
XM_006720991.2:c.4331T>C
|
XP_006721054.1:p.Met1444Thr
|
|
XM_006720992.2:c.1964T>C
|
XP_006721055.1:p.Met655Thr
|
|
XM_011522766.1:c.4085T>C
|
XP_011521068.1:p.Met1362Thr
|
|
XM_011522767.1:c.3356T>C
|
XP_011521069.1:p.Met1119Thr
|
|
XM_006720990.3:c.4331T>C
|
XP_006721053.1:p.Met1444Thr
|
|
XM_006720991.3:c.4331T>C
|
XP_006721054.1:p.Met1444Thr
|
|
XM_006720992.3:c.1964T>C
|
XP_006721055.1:p.Met655Thr
|
|
XM_011522766.3:c.4085T>C
|
XP_011521068.1:p.Met1362Thr
|
|
XM_011522767.2:c.3356T>C
|
XP_011521069.1:p.Met1119Thr
|
|
XM_017023910.1:c.4331T>C
|
XP_016879399.1:p.Met1444Thr
|
|
XM_017023911.1:c.2516T>C
|
XP_016879400.1:p.Met839Thr
|
|
NM_014714.4:c.4331T>C
MANE Select
|
NP_055529.2:p.Met1444Thr
|
|