ENST00000279873.12:c.733+19969T>G
MANE Select
|
ENSP00000279873.7:n.733+19969T>G
|
|
ENST00000644638.1:c.734-4383T>G
|
ENSP00000494412.1:n.734-4383T>G
|
|
ENST00000681100.1:c.733+19969T>G
|
ENSP00000506119.1:n.733+19969T>G
|
|
ENST00000279873.11:c.733+19969T>G
|
ENSP00000279873.7:n.733+19969T>G
|
|
NM_032199.2:c.733+19969T>G
|
NP_115575.1:n.733+19969T>G
|
|
XM_011540262.1:c.503-30598T>G
|
XP_011538564.1:n.503-30598T>G
|
|
XM_024448230.1:c.166+19969T>G
|
XP_024303998.1:n.166+19969T>G
|
|
NM_032199.3:c.733+19969T>G
MANE Select
|
NP_115575.1:n.733+19969T>G
|
|