ENST00000262367.10:c.6034G>T
MANE Select
|
ENSP00000262367.5:p.Val2012Phe
|
|
ENST00000262367.9:c.6034G>T
|
ENSP00000262367.5:p.Val2012Phe
|
|
ENST00000382070.7:c.5920G>T
|
ENSP00000371502.3:p.Val1974Phe
|
|
NM_001079846.1:c.5920G>T
|
NP_001073315.1:p.Val1974Phe
|
|
NM_004380.2:c.6034G>T
|
NP_004371.2:p.Val2012Phe
|
|
XM_005255124.3:c.5989G>T
|
XP_005255181.1:p.Val1997Phe
|
|
XM_005255125.3:c.5617G>T
|
XP_005255182.1:p.Val1873Phe
|
|
XM_006720848.2:c.5773G>T
|
XP_006720911.1:p.Val1925Phe
|
|
XM_011522380.1:c.5980G>T
|
XP_011520682.1:p.Val1994Phe
|
|
XM_011522381.1:c.5281G>T
|
XP_011520683.1:p.Val1761Phe
|
|
XM_005255124.4:c.5989G>T
|
XP_005255181.1:p.Val1997Phe
|
|
XM_005255125.4:c.5617G>T
|
XP_005255182.1:p.Val1873Phe
|
|
XM_006720848.3:c.5773G>T
|
XP_006720911.1:p.Val1925Phe
|
|
XM_011522381.2:c.5281G>T
|
XP_011520683.1:p.Val1761Phe
|
|
XM_017022944.1:c.6028G>T
|
XP_016878433.1:p.Val2010Phe
|
|
NM_004380.3:c.6034G>T
MANE Select
|
NP_004371.2:p.Val2012Phe
|
|