ENST00000376259.7:c.*1744C>A
MANE Select
|
ENSP00000365435.3:n.*1744C>A
|
|
ENST00000376259.6:c.*1744C>A
|
ENSP00000365435.3:n.*1744C>A
|
|
ENST00000492361.1:n.3119C>A
|
|
|
NM_001066.2:c.*1744C>A
|
NP_001057.1:n.*1744C>A
|
|
XM_011542060.1:c.*1744C>A
|
XP_011540362.1:n.*1744C>A
|
|
XM_011542061.1:c.*1744C>A
|
XP_011540363.1:n.*1744C>A
|
|
XM_011542062.1:c.3178C>A
|
XP_011540364.1:n.3178C>A
|
|
XM_011542063.1:c.*1744C>A
|
XP_011540365.1:n.*1744C>A
|
|
XM_011542060.2:c.*1744C>A
|
XP_011540362.1:n.*1744C>A
|
|
XM_011542063.2:c.*1744C>A
|
XP_011540365.1:n.*1744C>A
|
|
XM_017002214.1:c.*1744C>A
|
XP_016857703.1:n.*1744C>A
|
|
XM_017002215.1:c.*1744C>A
|
XP_016857704.1:n.*1744C>A
|
|
NM_001066.3:c.*1744C>A
MANE Select
|
NP_001057.1:n.*1744C>A
|
|