ENST00000389484.8:c.2888-11181T>C
MANE Select
|
ENSP00000374135.3:n.2888-11181T>C
|
|
ENST00000389484.7:c.2888-11181T>C
|
ENSP00000374135.3:n.2888-11181T>C
|
|
ENST00000434794.1:c.323-11181T>C
|
ENSP00000413239.1:n.323-11181T>C
|
|
ENST00000618808.4:c.2546-11181T>C
|
ENSP00000478868.1:n.2546-11181T>C
|
|
NM_018557.2:c.2888-11181T>C
|
NP_061027.2:n.2888-11181T>C
|
|
XM_011511352.1:c.2999-11181T>C
|
XP_011509654.1:n.2999-11181T>C
|
|
XM_017004341.1:c.2498-11181T>C
|
XP_016859830.1:n.2498-11181T>C
|
|
XR_001738778.1:n.4622-11181T>C
|
|
|
NM_018557.3:c.2888-11181T>C
MANE Select
|
NP_061027.2:n.2888-11181T>C
|
|