ENST00000263780.9:c.*231T>C
MANE Select
|
ENSP00000263780.4:n.*231T>C
|
|
ENST00000472024.3:c.*231T>C
|
ENSP00000480032.2:n.*231T>C
|
|
ENST00000676705.1:c.*231T>C
|
ENSP00000504098.1:n.*231T>C
|
|
ENST00000677929.1:n.4537T>C
|
|
|
ENST00000678859.1:n.4622T>C
|
|
|
ENST00000263780.8:c.*231T>C
|
ENSP00000263780.4:n.*231T>C
|
|
ENST00000471660.5:c.*231T>C
|
ENSP00000419998.1:n.*231T>C
|
|
ENST00000494980.5:c.*231T>C
|
ENSP00000418920.1:n.*231T>C
|
|
NM_001244644.1:c.*231T>C
|
NP_001231573.1:n.*231T>C
|
|
NM_014043.3:c.*231T>C
|
NP_054762.2:n.*231T>C
|
|
XM_011533576.1:c.*231T>C
|
XP_011531878.1:n.*231T>C
|
|
XM_011533576.2:c.*231T>C
|
XP_011531878.1:n.*231T>C
|
|
NM_014043.4:c.*231T>C
MANE Select
|
NP_054762.2:n.*231T>C
|
|
NM_001244644.2:c.*231T>C
|
NP_001231573.1:n.*231T>C
|
|