ENST00000382103.7:c.389-231G>C
MANE Select
|
ENSP00000371535.2:n.389-231G>C
|
|
ENST00000680581.1:c.389-231G>C
|
ENSP00000506483.1:n.389-231G>C
|
|
ENST00000680824.1:n.1605-231G>C
|
|
|
ENST00000681071.1:n.681-231G>C
|
|
|
ENST00000681166.1:n.1436-231G>C
|
|
|
ENST00000681341.1:n.1530-231G>C
|
|
|
ENST00000681640.1:n.483-231G>C
|
|
|
ENST00000681948.1:c.644-231G>C
|
ENSP00000505991.1:n.644-231G>C
|
|
ENST00000358971.7:c.*187-231G>C
|
ENSP00000351857.3:n.*187-231G>C
|
|
ENST00000382103.6:c.389-231G>C
|
ENSP00000371535.2:n.389-231G>C
|
|
ENST00000514585.5:c.*90-231G>C
|
ENSP00000421880.1:n.*90-231G>C
|
|
NM_016955.3:c.389-231G>C
|
NP_058651.3:n.389-231G>C
|
|
XM_005248168.2:c.152-231G>C
|
XP_005248225.1:n.152-231G>C
|
|
XM_006713965.2:c.209-231G>C
|
XP_006714028.1:n.209-231G>C
|
|
XM_011513846.1:c.386-231G>C
|
XP_011512148.1:n.386-231G>C
|
|
XM_011513847.1:c.356-231G>C
|
XP_011512149.1:n.356-231G>C
|
|
XM_011513848.1:c.209-231G>C
|
XP_011512150.1:n.209-231G>C
|
|
XM_011513846.2:c.386-231G>C
|
XP_011512148.1:n.386-231G>C
|
|
XM_011513847.2:c.356-231G>C
|
XP_011512149.1:n.356-231G>C
|
|
XM_017008277.1:c.644-231G>C
|
XP_016863766.1:n.644-231G>C
|
|
XM_017008278.1:c.-35-231G>C
|
XP_016863767.1:n.-35-231G>C
|
|
NM_016955.4:c.389-231G>C
MANE Select
|
NP_058651.3:n.389-231G>C
|
|