ENST00000262367.10:c.4462C>T
MANE Select
|
ENSP00000262367.5:p.Pro1488Ser
|
|
ENST00000262367.9:c.4462C>T
|
ENSP00000262367.5:p.Pro1488Ser
|
|
ENST00000382070.7:c.4348C>T
|
ENSP00000371502.3:p.Pro1450Ser
|
|
ENST00000570939.2:c.3097C>T
|
ENSP00000461002.2:p.Pro1033Ser
|
|
ENST00000571763.5:n.252C>T
|
|
|
ENST00000574740.1:n.283C>T
|
|
|
ENST00000576720.1:n.3285C>T
|
|
|
NM_001079846.1:c.4348C>T
|
NP_001073315.1:p.Pro1450Ser
|
|
NM_004380.2:c.4462C>T
|
NP_004371.2:p.Pro1488Ser
|
|
XM_005255124.3:c.4417C>T
|
XP_005255181.1:p.Pro1473Ser
|
|
XM_005255125.3:c.4045C>T
|
XP_005255182.1:p.Pro1349Ser
|
|
XM_006720848.2:c.4201C>T
|
XP_006720911.1:p.Pro1401Ser
|
|
XM_011522380.1:c.4408C>T
|
XP_011520682.1:p.Pro1470Ser
|
|
XM_011522381.1:c.3709C>T
|
XP_011520683.1:p.Pro1237Ser
|
|
XM_005255124.4:c.4417C>T
|
XP_005255181.1:p.Pro1473Ser
|
|
XM_005255125.4:c.4045C>T
|
XP_005255182.1:p.Pro1349Ser
|
|
XM_006720848.3:c.4201C>T
|
XP_006720911.1:p.Pro1401Ser
|
|
XM_011522381.2:c.3709C>T
|
XP_011520683.1:p.Pro1237Ser
|
|
XM_017022944.1:c.4456C>T
|
XP_016878433.1:p.Pro1486Ser
|
|
NM_004380.3:c.4462C>T
MANE Select
|
NP_004371.2:p.Pro1488Ser
|
|