ENST00000375263.8:c.*152T>C
MANE Select
|
ENSP00000364412.3:n.*152T>C
|
|
ENST00000494814.6:n.635T>C
|
|
|
ENST00000375262.3:c.*152T>C
|
ENSP00000364411.2:n.*152T>C
|
|
ENST00000375263.7:c.*152T>C
|
ENSP00000364412.3:n.*152T>C
|
|
ENST00000464104.5:n.938T>C
|
|
|
ENST00000467499.5:n.345T>C
|
|
|
ENST00000494814.5:n.644T>C
|
|
|
NM_000197.1:c.*152T>C
|
NP_000188.1:n.*152T>C
|
|
XM_005251970.3:c.*152T>C
|
XP_005252027.1:n.*152T>C
|
|
XM_011518618.1:c.*152T>C
|
XP_011516920.1:n.*152T>C
|
|
XM_011518619.1:c.*152T>C
|
XP_011516921.1:n.*152T>C
|
|
XM_011518620.1:c.*152T>C
|
XP_011516922.1:n.*152T>C
|
|
NM_000197.2:c.*152T>C
MANE Select
|
NP_000188.1:n.*152T>C
|
|
XM_011518618.2:c.*152T>C
|
XP_011516920.1:n.*152T>C
|
|
XM_011518619.2:c.*152T>C
|
XP_011516921.1:n.*152T>C
|
|
XM_017014671.1:c.*152T>C
|
XP_016870160.1:n.*152T>C
|
|
XM_017014672.1:c.*152T>C
|
XP_016870161.1:n.*152T>C
|
|
XM_017014673.2:c.*152T>C
|
XP_016870162.1:n.*152T>C
|
|
XM_017014674.1:c.*152T>C
|
XP_016870163.1:n.*152T>C
|
|
XM_017014675.1:c.*152T>C
|
XP_016870164.1:n.*152T>C
|
|
XM_017014677.1:c.*152T>C
|
XP_016870166.1:n.*152T>C
|
|
XM_024447529.1:c.*152T>C
|
XP_024303297.1:n.*152T>C
|
|
XR_002956778.1:n.3557T>C
|
|
|