ENST00000449606.7:c.*1808G>A
MANE Select
|
ENSP00000395196.2:n.*1808G>A
|
|
ENST00000674054.1:c.*1715G>A
|
ENSP00000501251.1:n.*1715G>A
|
|
ENST00000449606.5:c.*1808G>A
|
ENSP00000395196.1:n.*1808G>A
|
|
ENST00000563459.5:c.*1715G>A
|
ENSP00000456467.1:n.*1715G>A
|
|
NM_001083614.1:c.*1808G>A
|
NP_001077083.1:n.*1808G>A
|
|
NR_003501.1:n.3319G>A
|
|
|
XM_011545738.1:c.*1808G>A
|
XP_011544040.1:n.*1808G>A
|
|
XM_011545739.1:c.*1808G>A
|
XP_011544041.1:n.*1808G>A
|
|
XR_001751841.1:n.3609G>A
|
|
|
NM_001083614.2:c.*1808G>A
MANE Select
|
NP_001077083.1:n.*1808G>A
|
|
NR_003501.2:n.3294G>A
|
|
|