ENST00000710380.1:c.1022-346T>C
|
ENSP00000518237.1:n.1022-346T>C
|
|
ENST00000371627.5:c.983-346T>C
MANE Select
|
ENSP00000360689.4:n.983-346T>C
|
|
ENST00000371627.4:c.983-346T>C
|
ENSP00000360689.4:n.983-346T>C
|
|
NM_025235.3:c.983-346T>C
|
NP_079511.1:n.983-346T>C
|
|
XM_011540213.1:c.1046-346T>C
|
XP_011538515.1:n.1046-346T>C
|
|
XM_011540214.1:c.407-346T>C
|
XP_011538516.1:n.407-346T>C
|
|
XM_005270185.4:c.1046-346T>C
|
XP_005270242.2:n.1046-346T>C
|
|
XM_017016696.1:c.983-346T>C
|
XP_016872185.1:n.983-346T>C
|
|
XM_017016697.1:c.662-346T>C
|
XP_016872186.1:n.662-346T>C
|
|
XM_017016698.2:c.662-346T>C
|
XP_016872187.1:n.662-346T>C
|
|
XM_017016699.1:c.662-346T>C
|
XP_016872188.1:n.662-346T>C
|
|
XM_017016700.2:c.407-346T>C
|
XP_016872189.1:n.407-346T>C
|
|
XM_017016701.1:c.1046-346T>C
|
XP_016872190.1:n.1046-346T>C
|
|
NM_025235.4:c.983-346T>C
MANE Select
|
NP_079511.1:n.983-346T>C
|
|