ENST00000285968.11:c.5684-143T>C
MANE Select
|
ENSP00000285968.6:n.5684-143T>C
|
|
ENST00000285968.10:c.5684-143T>C
|
ENSP00000285968.6:n.5684-143T>C
|
|
ENST00000461255.5:n.891-143T>C
|
|
|
ENST00000477620.5:c.1405+347T>C
|
|
|
ENST00000490439.1:c.120+307T>C
|
|
|
ENST00000607647.5:n.3962-143T>C
|
|
|
NM_015135.2:c.5684-143T>C
|
NP_055950.1:n.5684-143T>C
|
|
XM_005250235.2:c.4610-143T>C
|
XP_005250292.1:n.4610-143T>C
|
|
NM_001329434.1:c.4610-143T>C
|
NP_001316363.1:n.4610-143T>C
|
|
NM_015135.3:c.5684-143T>C
MANE Select
|
NP_055950.2:n.5684-143T>C
|
|
NM_001329434.2:c.4610-143T>C
|
NP_001316363.2:n.4610-143T>C
|
|