ENST00000449742.7:c.*1729C>T
MANE Select
|
ENSP00000397073.2:n.*1729C>T
|
|
ENST00000376704.3:c.*1448C>T
|
ENSP00000365894.3:n.*1448C>T
|
|
ENST00000449742.6:c.*1729C>T
|
ENSP00000397073.2:n.*1729C>T
|
|
NM_006778.3:c.*1729C>T
|
NP_006769.2:n.*1729C>T
|
|
NM_052828.2:c.*1448C>T
|
NP_439893.2:n.*1448C>T
|
|
XM_011514221.1:c.*1729C>T
|
XP_011512523.1:n.*1729C>T
|
|
XM_011514222.1:c.*1729C>T
|
XP_011512524.1:n.*1729C>T
|
|
XM_011514223.1:c.*1729C>T
|
XP_011512525.1:n.*1729C>T
|
|
XM_011514224.1:c.*1729C>T
|
XP_011512526.1:n.*1729C>T
|
|
XM_011514225.1:c.*1448C>T
|
XP_011512527.1:n.*1448C>T
|
|
XM_011514222.2:c.*1729C>T
|
XP_011512524.1:n.*1729C>T
|
|
XM_011514223.2:c.*1729C>T
|
XP_011512525.1:n.*1729C>T
|
|
NM_006778.4:c.*1729C>T
MANE Select
|
NP_006769.2:n.*1729C>T
|
|
NM_052828.3:c.*1448C>T
|
NP_439893.2:n.*1448C>T
|
|