ENST00000331849.8:c.1536+922C>A
MANE Select
|
ENSP00000327916.4:n.1536+922C>A
|
|
ENST00000577024.1:n.449+922C>A
|
|
|
NM_017888.2:c.1536+922C>A
|
NP_060358.2:n.1536+922C>A
|
|
XM_006721055.2:c.1536+922C>A
|
XP_006721118.1:n.1536+922C>A
|
|
XM_006721056.2:c.1536+922C>A
|
XP_006721119.1:n.1536+922C>A
|
|
NM_001324371.1:c.1536+922C>A
|
NP_001311300.1:n.1536+922C>A
|
|
NM_001324372.1:c.1536+922C>A
|
NP_001311301.1:n.1536+922C>A
|
|
NM_017888.3:c.1536+922C>A
MANE Select
|
NP_060358.2:n.1536+922C>A
|
|
NM_001324371.2:c.1536+922C>A
|
NP_001311300.1:n.1536+922C>A
|
|
NM_001324372.2:c.1536+922C>A
|
NP_001311301.1:n.1536+922C>A
|
|