ENST00000262367.10:c.5186G>T
MANE Select
|
ENSP00000262367.5:p.Cys1729Phe
|
|
ENST00000262367.9:c.5186G>T
|
ENSP00000262367.5:p.Cys1729Phe
|
|
ENST00000382070.7:c.5072G>T
|
ENSP00000371502.3:p.Cys1691Phe
|
|
NM_001079846.1:c.5072G>T
|
NP_001073315.1:p.Cys1691Phe
|
|
NM_004380.2:c.5186G>T
|
NP_004371.2:p.Cys1729Phe
|
|
XM_005255124.3:c.5141G>T
|
XP_005255181.1:p.Cys1714Phe
|
|
XM_005255125.3:c.4769G>T
|
XP_005255182.1:p.Cys1590Phe
|
|
XM_006720848.2:c.4925G>T
|
XP_006720911.1:p.Cys1642Phe
|
|
XM_011522380.1:c.5132G>T
|
XP_011520682.1:p.Cys1711Phe
|
|
XM_011522381.1:c.4433G>T
|
XP_011520683.1:p.Cys1478Phe
|
|
XM_005255124.4:c.5141G>T
|
XP_005255181.1:p.Cys1714Phe
|
|
XM_005255125.4:c.4769G>T
|
XP_005255182.1:p.Cys1590Phe
|
|
XM_006720848.3:c.4925G>T
|
XP_006720911.1:p.Cys1642Phe
|
|
XM_011522381.2:c.4433G>T
|
XP_011520683.1:p.Cys1478Phe
|
|
XM_017022944.1:c.5180G>T
|
XP_016878433.1:p.Cys1727Phe
|
|
NM_004380.3:c.5186G>T
MANE Select
|
NP_004371.2:p.Cys1729Phe
|
|