ENST00000262367.10:c.7297G>T
MANE Select
|
ENSP00000262367.5:p.Asp2433Tyr
|
|
ENST00000262367.9:c.7297G>T
|
ENSP00000262367.5:p.Asp2433Tyr
|
|
ENST00000382070.7:c.7183G>T
|
ENSP00000371502.3:p.Asp2395Tyr
|
|
NM_001079846.1:c.7183G>T
|
NP_001073315.1:p.Asp2395Tyr
|
|
NM_004380.2:c.7297G>T
|
NP_004371.2:p.Asp2433Tyr
|
|
XM_005255124.3:c.7252G>T
|
XP_005255181.1:p.Asp2418Tyr
|
|
XM_005255125.3:c.6880G>T
|
XP_005255182.1:p.Asp2294Tyr
|
|
XM_006720848.2:c.7036G>T
|
XP_006720911.1:p.Asp2346Tyr
|
|
XM_011522380.1:c.7243G>T
|
XP_011520682.1:p.Asp2415Tyr
|
|
XM_011522381.1:c.6544G>T
|
XP_011520683.1:p.Asp2182Tyr
|
|
XM_005255124.4:c.7252G>T
|
XP_005255181.1:p.Asp2418Tyr
|
|
XM_005255125.4:c.6880G>T
|
XP_005255182.1:p.Asp2294Tyr
|
|
XM_006720848.3:c.7036G>T
|
XP_006720911.1:p.Asp2346Tyr
|
|
XM_011522381.2:c.6544G>T
|
XP_011520683.1:p.Asp2182Tyr
|
|
XM_017022944.1:c.7291G>T
|
XP_016878433.1:p.Asp2431Tyr
|
|
NM_004380.3:c.7297G>T
MANE Select
|
NP_004371.2:p.Asp2433Tyr
|
|