ENST00000262367.10:c.6940A=
MANE Select
|
ENSP00000262367.5:p.Met2314=
|
|
ENST00000262367.9:c.6940A=
|
ENSP00000262367.5:p.Met2314=
|
|
ENST00000382070.7:c.6826A=
|
ENSP00000371502.3:p.Met2276=
|
|
NM_001079846.1:c.6826A=
|
NP_001073315.1:p.Met2276=
|
|
NM_004380.2:c.6940A=
|
NP_004371.2:p.Met2314=
|
|
XM_005255124.3:c.6895A=
|
XP_005255181.1:p.Met2299=
|
|
XM_005255125.3:c.6523A=
|
XP_005255182.1:p.Met2175=
|
|
XM_006720848.2:c.6679A=
|
XP_006720911.1:p.Met2227=
|
|
XM_011522380.1:c.6886A=
|
XP_011520682.1:p.Met2296=
|
|
XM_011522381.1:c.6187A=
|
XP_011520683.1:p.Met2063=
|
|
XM_005255124.4:c.6895A=
|
XP_005255181.1:p.Met2299=
|
|
XM_005255125.4:c.6523A=
|
XP_005255182.1:p.Met2175=
|
|
XM_006720848.3:c.6679A=
|
XP_006720911.1:p.Met2227=
|
|
XM_011522381.2:c.6187A=
|
XP_011520683.1:p.Met2063=
|
|
XM_017022944.1:c.6934A=
|
XP_016878433.1:p.Met2312=
|
|
NM_004380.3:c.6940A=
MANE Select
|
NP_004371.2:p.Met2314=
|
|