ENST00000703637.1:c.*1934T>C
|
ENSP00000515413.1:n.*1934T>C
|
|
ENST00000360864.9:c.*1767T>C
MANE Select
|
ENSP00000354111.4:n.*1767T>C
|
|
ENST00000360864.8:c.*1767T>C
|
ENSP00000354111.4:n.*1767T>C
|
|
ENST00000470551.1:c.*1934T>C
|
ENSP00000434744.1:n.*1934T>C
|
|
NM_025219.2:c.*1767T>C
|
NP_079495.1:n.*1767T>C
|
|
XM_011529048.1:c.*1767T>C
|
XP_011527350.1:n.*1767T>C
|
|
XM_011529049.1:c.*1767T>C
|
XP_011527351.1:n.*1767T>C
|
|
XM_011529050.1:c.*1767T>C
|
XP_011527352.1:n.*1767T>C
|
|
XR_936629.1:n.3070T>C
|
|
|
XR_936630.1:n.3328T>C
|
|
|
XM_011529048.2:c.*1767T>C
|
XP_011527350.1:n.*1767T>C
|
|
XR_936629.2:n.3083T>C
|
|
|
NM_025219.3:c.*1767T>C
MANE Select
|
NP_079495.1:n.*1767T>C
|
|