ENST00000389484.8:c.1789+11121C>G
MANE Select
|
ENSP00000374135.3:n.1789+11121C>G
|
|
ENST00000389484.7:c.1789+11121C>G
|
ENSP00000374135.3:n.1789+11121C>G
|
|
ENST00000434794.1:c.206-55589C>G
|
ENSP00000413239.1:n.206-55589C>G
|
|
ENST00000618808.4:c.1447+11121C>G
|
ENSP00000478868.1:n.1447+11121C>G
|
|
NM_018557.2:c.1789+11121C>G
|
NP_061027.2:n.1789+11121C>G
|
|
XM_011511352.1:c.1900+11121C>G
|
XP_011509654.1:n.1900+11121C>G
|
|
XM_017004341.1:c.1399+11121C>G
|
XP_016859830.1:n.1399+11121C>G
|
|
XR_001738778.1:n.3523+11121C>G
|
|
|
NM_018557.3:c.1789+11121C>G
MANE Select
|
NP_061027.2:n.1789+11121C>G
|
|