ENST00000298139.7:c.*3T>C
MANE Select
|
ENSP00000298139.5:n.*3T>C
|
|
ENST00000650667.1:c.*3916T>C
|
ENSP00000498593.1:n.*3916T>C
|
|
ENST00000651946.1:n.526T>C
|
|
|
ENST00000298139.5:c.*3T>C
|
ENSP00000298139.5:n.*3T>C
|
|
ENST00000521620.5:n.2935T>C
|
|
|
NM_000553.4:c.*3T>C , LRG_524t1:c.*3T>C
|
NP_000544.2:n.*3T>C
|
|
XM_011544639.1:c.*3T>C
|
XP_011542941.1:n.*3T>C
|
|
XM_011544640.1:c.*3T>C
|
XP_011542942.1:n.*3T>C
|
|
XR_949643.1:n.88-1787A>G
|
|
|
XR_949644.1:n.88-1787A>G
|
|
|
XR_949645.1:n.88-1787A>G
|
|
|
XR_949646.1:n.88-1787A>G
|
|
|
XR_949647.1:n.701-1787A>G
|
|
|
XR_949648.1:n.603-1787A>G
|
|
|
NM_000553.5:c.*3T>C
|
NP_000544.2:n.*3T>C
|
|
XM_011544639.3:c.*3T>C
|
XP_011542941.1:n.*3T>C
|
|
XM_024447265.1:c.*3T>C
|
XP_024303033.1:n.*3T>C
|
|
NM_000553.6:c.*3T>C
MANE Select
|
NP_000544.2:n.*3T>C
|
|