ENST00000382103.7:c.947C>T
MANE Select
|
ENSP00000371535.2:p.Ala316Val
|
|
ENST00000680581.1:c.947C>T
|
ENSP00000506483.1:p.Ala316Val
|
|
ENST00000680824.1:n.2163C>T
|
|
|
ENST00000681071.1:n.1239C>T
|
|
|
ENST00000681341.1:n.2088C>T
|
|
|
ENST00000681948.1:c.1202C>T
|
ENSP00000505991.1:p.Ala401Val
|
|
ENST00000358971.7:c.*745C>T
|
ENSP00000351857.3:n.*745C>T
|
|
ENST00000382103.6:c.947C>T
|
ENSP00000371535.2:p.Ala316Val
|
|
ENST00000503150.1:c.229C>T
|
|
|
ENST00000505513.1:n.247C>T
|
|
|
ENST00000514585.5:c.*648C>T
|
ENSP00000421880.1:n.*648C>T
|
|
NM_016955.3:c.947C>T
|
NP_058651.3:p.Ala316Val
|
|
XM_005248168.2:c.710C>T
|
XP_005248225.1:p.Ala237Val
|
|
XM_006713965.2:c.767C>T
|
XP_006714028.1:p.Ala256Val
|
|
XM_011513846.1:c.944C>T
|
XP_011512148.1:p.Ala315Val
|
|
XM_011513847.1:c.914C>T
|
XP_011512149.1:p.Ala305Val
|
|
XM_011513848.1:c.767C>T
|
XP_011512150.1:p.Ala256Val
|
|
XM_011513846.2:c.944C>T
|
XP_011512148.1:p.Ala315Val
|
|
XM_011513847.2:c.914C>T
|
XP_011512149.1:p.Ala305Val
|
|
XM_017008277.1:c.1202C>T
|
XP_016863766.1:p.Ala401Val
|
|
XM_017008278.1:c.524C>T
|
XP_016863767.1:p.Ala175Val
|
|
NM_016955.4:c.947C>T
MANE Select
|
NP_058651.3:p.Ala316Val
|
|