ENST00000262367.10:c.5825T>C
MANE Select
|
ENSP00000262367.5:p.Val1942Ala
|
|
ENST00000262367.9:c.5825T>C
|
ENSP00000262367.5:p.Val1942Ala
|
|
ENST00000382070.7:c.5711T>C
|
ENSP00000371502.3:p.Val1904Ala
|
|
NM_001079846.1:c.5711T>C
|
NP_001073315.1:p.Val1904Ala
|
|
NM_004380.2:c.5825T>C
|
NP_004371.2:p.Val1942Ala
|
|
XM_005255124.3:c.5780T>C
|
XP_005255181.1:p.Val1927Ala
|
|
XM_005255125.3:c.5408T>C
|
XP_005255182.1:p.Val1803Ala
|
|
XM_006720848.2:c.5564T>C
|
XP_006720911.1:p.Val1855Ala
|
|
XM_011522380.1:c.5771T>C
|
XP_011520682.1:p.Val1924Ala
|
|
XM_011522381.1:c.5072T>C
|
XP_011520683.1:p.Val1691Ala
|
|
XM_005255124.4:c.5780T>C
|
XP_005255181.1:p.Val1927Ala
|
|
XM_005255125.4:c.5408T>C
|
XP_005255182.1:p.Val1803Ala
|
|
XM_006720848.3:c.5564T>C
|
XP_006720911.1:p.Val1855Ala
|
|
XM_011522381.2:c.5072T>C
|
XP_011520683.1:p.Val1691Ala
|
|
XM_017022944.1:c.5819T>C
|
XP_016878433.1:p.Val1940Ala
|
|
NM_004380.3:c.5825T>C
MANE Select
|
NP_004371.2:p.Val1942Ala
|
|