ENST00000318471.5:c.803+269C>T
MANE Select
|
ENSP00000315680.3:n.803+269C>T
|
|
ENST00000541292.6:c.*68+269C>T
|
ENSP00000441004.1:n.*68+269C>T
|
|
ENST00000678002.1:c.491+269C>T
|
|
|
ENST00000678557.1:c.689+269C>T
|
ENSP00000502962.1:n.689+269C>T
|
|
ENST00000678593.1:c.1077C>T
|
ENSP00000503841.1:n.1077C>T
|
|
ENST00000679286.1:c.683+269C>T
|
ENSP00000503168.1:n.683+269C>T
|
|
ENST00000318471.4:c.803+269C>T
|
ENSP00000315680.3:n.803+269C>T
|
|
NM_000288.3:c.803+269C>T
|
NP_000279.1:n.803+269C>T
|
|
XM_005267019.3:c.689+269C>T
|
XP_005267076.1:n.689+269C>T
|
|
XM_006715502.1:c.509+269C>T
|
XP_006715565.1:n.509+269C>T
|
|
XM_011535900.1:c.527-25620C>T
|
XP_011534202.1:n.527-25620C>T
|
|
XM_005267019.4:c.689+269C>T
|
XP_005267076.1:n.689+269C>T
|
|
XM_006715502.2:c.509+269C>T
|
XP_006715565.1:n.509+269C>T
|
|
XM_017010934.2:c.527-25620C>T
|
XP_016866423.1:n.527-25620C>T
|
|
NM_000288.4:c.803+269C>T
MANE Select
|
NP_000279.1:n.803+269C>T
|
|