ENST00000262367.10:c.7089G>A
MANE Select
|
ENSP00000262367.5:p.Pro2363=
|
|
ENST00000262367.9:c.7089G>A
|
ENSP00000262367.5:p.Pro2363=
|
|
ENST00000382070.7:c.6975G>A
|
ENSP00000371502.3:p.Pro2325=
|
|
NM_001079846.1:c.6975G>A
|
NP_001073315.1:p.Pro2325=
|
|
NM_004380.2:c.7089G>A
|
NP_004371.2:p.Pro2363=
|
|
XM_005255124.3:c.7044G>A
|
XP_005255181.1:p.Pro2348=
|
|
XM_005255125.3:c.6672G>A
|
XP_005255182.1:p.Pro2224=
|
|
XM_006720848.2:c.6828G>A
|
XP_006720911.1:p.Pro2276=
|
|
XM_011522380.1:c.7035G>A
|
XP_011520682.1:p.Pro2345=
|
|
XM_011522381.1:c.6336G>A
|
XP_011520683.1:p.Pro2112=
|
|
XM_005255124.4:c.7044G>A
|
XP_005255181.1:p.Pro2348=
|
|
XM_005255125.4:c.6672G>A
|
XP_005255182.1:p.Pro2224=
|
|
XM_006720848.3:c.6828G>A
|
XP_006720911.1:p.Pro2276=
|
|
XM_011522381.2:c.6336G>A
|
XP_011520683.1:p.Pro2112=
|
|
XM_017022944.1:c.7083G>A
|
XP_016878433.1:p.Pro2361=
|
|
NM_004380.3:c.7089G>A
MANE Select
|
NP_004371.2:p.Pro2363=
|
|