ENST00000262367.10:c.5477G>T
MANE Select
|
ENSP00000262367.5:p.Cys1826Phe
|
|
ENST00000262367.9:c.5477G>T
|
ENSP00000262367.5:p.Cys1826Phe
|
|
ENST00000382070.7:c.5363G>T
|
ENSP00000371502.3:p.Cys1788Phe
|
|
NM_001079846.1:c.5363G>T
|
NP_001073315.1:p.Cys1788Phe
|
|
NM_004380.2:c.5477G>T
|
NP_004371.2:p.Cys1826Phe
|
|
XM_005255124.3:c.5432G>T
|
XP_005255181.1:p.Cys1811Phe
|
|
XM_005255125.3:c.5060G>T
|
XP_005255182.1:p.Cys1687Phe
|
|
XM_006720848.2:c.5216G>T
|
XP_006720911.1:p.Cys1739Phe
|
|
XM_011522380.1:c.5423G>T
|
XP_011520682.1:p.Cys1808Phe
|
|
XM_011522381.1:c.4724G>T
|
XP_011520683.1:p.Cys1575Phe
|
|
XM_005255124.4:c.5432G>T
|
XP_005255181.1:p.Cys1811Phe
|
|
XM_005255125.4:c.5060G>T
|
XP_005255182.1:p.Cys1687Phe
|
|
XM_006720848.3:c.5216G>T
|
XP_006720911.1:p.Cys1739Phe
|
|
XM_011522381.2:c.4724G>T
|
XP_011520683.1:p.Cys1575Phe
|
|
XM_017022944.1:c.5471G>T
|
XP_016878433.1:p.Cys1824Phe
|
|
NM_004380.3:c.5477G>T
MANE Select
|
NP_004371.2:p.Cys1826Phe
|
|