|
NM_003860.4:c.*143T>A
MANE Select
|
NP_003851.1:n.*143T>A
|
|
ENST00000312175.7:c.*143T>A
MANE Select
|
ENSP00000310275.2:n.*143T>A
|
|
NM_001143985.1:c.*143T>A
|
NP_001137457.1:n.*143T>A
|
|
NM_003860.3:c.*143T>A
|
NP_003851.1:n.*143T>A
|
|
ENST00000312175.6:c.*143T>A
|
ENSP00000310275.2:n.*143T>A
|
|
ENST00000445560.6:c.*143T>A
|
ENSP00000416128.2:n.*143T>A
|
|
ENST00000524628.1:n.381T>A
|
|
|
ENST00000533166.5:c.*143T>A
|
ENSP00000433760.1:n.*143T>A
|
|
XM_017018514.1:c.*143T>A
|
XP_016874003.1:n.*143T>A
|
|
XM_017018515.2:c.*143T>A
|
XP_016874004.1:n.*143T>A
|