|
NM_006420.3:c.*1876G>A
MANE Select
|
NP_006411.2:n.*1876G>A
|
|
ENST00000371917.5:c.*1876G>A
MANE Select
|
ENSP00000360985.4:n.*1876G>A
|
|
NM_006420.2:c.*1876G>A
|
NP_006411.2:n.*1876G>A
|
|
ENST00000371917.4:c.7234G>A
|
ENSP00000360985.4:n.7234G>A
|
|
ENST00000679436.1:c.7231G>A
|
ENSP00000504888.1:n.7231G>A
|
|
ENST00000679542.1:n.6923G>A
|
|
|
ENST00000680130.1:n.2905G>A
|
|
|
ENST00000681119.1:n.3968G>A
|
|
|
ENST00000681399.1:c.*6911G>A
|
ENSP00000506363.1:n.*6911G>A
|
|
XM_005260252.2:c.*1876G>A
|
XP_005260309.1:n.*1876G>A
|
|
XM_005260252.3:c.*1876G>A
|
XP_005260309.1:n.*1876G>A
|