ENST00000382103.7:c.386C>T
MANE Select
|
ENSP00000371535.2:p.Ala129Val
|
|
ENST00000680581.1:c.386C>T
|
ENSP00000506483.1:p.Ala129Val
|
|
ENST00000680824.1:n.1602C>T
|
|
|
ENST00000681071.1:n.678C>T
|
|
|
ENST00000681166.1:n.1433C>T
|
|
|
ENST00000681341.1:n.1527C>T
|
|
|
ENST00000681640.1:n.480C>T
|
|
|
ENST00000681948.1:c.641C>T
|
ENSP00000505991.1:p.Ala214Val
|
|
ENST00000358971.7:c.*184C>T
|
ENSP00000351857.3:n.*184C>T
|
|
ENST00000382103.6:c.386C>T
|
ENSP00000371535.2:p.Ala129Val
|
|
ENST00000514585.5:c.*87C>T
|
ENSP00000421880.1:n.*87C>T
|
|
NM_016955.3:c.386C>T
|
NP_058651.3:p.Ala129Val
|
|
XM_005248168.2:c.149C>T
|
XP_005248225.1:p.Ala50Val
|
|
XM_006713965.2:c.206C>T
|
XP_006714028.1:p.Ala69Val
|
|
XM_011513846.1:c.383C>T
|
XP_011512148.1:p.Ala128Val
|
|
XM_011513847.1:c.353C>T
|
XP_011512149.1:p.Ala118Val
|
|
XM_011513848.1:c.206C>T
|
XP_011512150.1:p.Ala69Val
|
|
XM_011513846.2:c.383C>T
|
XP_011512148.1:p.Ala128Val
|
|
XM_011513847.2:c.353C>T
|
XP_011512149.1:p.Ala118Val
|
|
XM_017008277.1:c.641C>T
|
XP_016863766.1:p.Ala214Val
|
|
XM_017008278.1:c.-38C>T
|
XP_016863767.1:n.-38C>T
|
|
NM_016955.4:c.386C>T
MANE Select
|
NP_058651.3:p.Ala129Val
|
|