ENST00000263780.9:c.*513A>T
MANE Select
|
ENSP00000263780.4:n.*513A>T
|
|
ENST00000472024.3:c.*513A>T
|
ENSP00000480032.2:n.*513A>T
|
|
ENST00000676705.1:c.*513A>T
|
ENSP00000504098.1:n.*513A>T
|
|
ENST00000677929.1:n.4819A>T
|
|
|
ENST00000678859.1:n.4904A>T
|
|
|
ENST00000263780.8:c.*513A>T
|
ENSP00000263780.4:n.*513A>T
|
|
ENST00000471660.5:c.*513A>T
|
ENSP00000419998.1:n.*513A>T
|
|
NM_001244644.1:c.*513A>T
|
NP_001231573.1:n.*513A>T
|
|
NM_014043.3:c.*513A>T
|
NP_054762.2:n.*513A>T
|
|
XM_011533576.1:c.*513A>T
|
XP_011531878.1:n.*513A>T
|
|
XM_011533576.2:c.*513A>T
|
XP_011531878.1:n.*513A>T
|
|
NM_014043.4:c.*513A>T
MANE Select
|
NP_054762.2:n.*513A>T
|
|
NM_001244644.2:c.*513A>T
|
NP_001231573.1:n.*513A>T
|
|