|
NM_014423.4:c.*1971T>A
MANE Select
|
NP_055238.1:n.*1971T>A
|
|
ENST00000265343.10:c.*1971T>A
MANE Select
|
ENSP00000265343.5:n.*1971T>A
|
|
NM_014423.3:c.*1971T>A
|
NP_055238.1:n.*1971T>A
|
|
ENST00000265343.9:c.*1971T>A
|
ENSP00000265343.5:n.*1971T>A
|
|
XM_005271963.3:c.*1971T>A
|
XP_005272020.1:n.*1971T>A
|
|
XM_005271963.5:c.*1971T>A
|
XP_005272020.1:n.*1971T>A
|
|
XM_005271964.3:c.*1971T>A
|
XP_005272021.1:n.*1971T>A
|
|
XM_005271964.4:c.*1971T>A
|
XP_005272021.1:n.*1971T>A
|
|
XM_006714587.2:c.*1971T>A
|
XP_006714650.1:n.*1971T>A
|
|
XM_006714587.4:c.*1971T>A
|
XP_006714650.1:n.*1971T>A
|