ENST00000342741.6:c.1619-273A>G
MANE Select
|
ENSP00000339933.4:n.1619-273A>G
|
|
ENST00000342741.4:c.1619-273A>G
|
ENSP00000339933.4:n.1619-273A>G
|
|
ENST00000392414.7:c.1526-273A>G
|
ENSP00000376214.3:n.1526-273A>G
|
|
NM_000298.5:c.1619-273A>G
|
NP_000289.1:n.1619-273A>G
|
|
NM_181871.3:c.1526-273A>G
|
NP_870986.1:n.1526-273A>G
|
|
XM_005245266.3:c.1778-273A>G
|
XP_005245323.1:n.1778-273A>G
|
|
XM_006711386.2:c.1427-273A>G
|
XP_006711449.1:n.1427-273A>G
|
|
XM_011509640.1:c.1427-273A>G
|
XP_011507942.1:n.1427-273A>G
|
|
NM_000298.6:c.1619-273A>G
MANE Select
|
NP_000289.1:n.1619-273A>G
|
|
XM_006711386.4:c.1427-273A>G
|
XP_006711449.1:n.1427-273A>G
|
|
XM_011509640.3:c.1427-273A>G
|
XP_011507942.1:n.1427-273A>G
|
|
NM_181871.4:c.1526-273A>G
|
NP_870986.1:n.1526-273A>G
|
|