ENST00000376261.8:c.1158-2757C>G
MANE Select
|
ENSP00000365437.3:n.1158-2757C>G
|
|
ENST00000648567.1:c.816-2757C>G
|
ENSP00000498009.1:n.816-2757C>G
|
|
ENST00000259271.7:c.1158-2757C>G
|
ENSP00000259271.3:n.1158-2757C>G
|
|
ENST00000376261.7:c.1158-2757C>G
|
ENSP00000365437.3:n.1158-2757C>G
|
|
NM_000818.2:c.1158-2757C>G
|
NP_000809.1:n.1158-2757C>G
|
|
NM_001134366.1:c.1158-2757C>G
|
NP_001127838.1:n.1158-2757C>G
|
|
NM_001134366.2:c.1158-2757C>G
MANE Select
|
NP_001127838.1:n.1158-2757C>G
|
|
NM_000818.3:c.1158-2757C>G
|
NP_000809.1:n.1158-2757C>G
|
|