|
ENST00000370192.8:c.150+2T>A
MANE Select
|
ENSP00000359211.3:n.150+2T>A
|
|
|
ENST00000306031.5:c.150+2T>A
|
ENSP00000307107.5:n.150+2T>A
|
|
|
ENST00000370192.7:c.150+2T>A
|
ENSP00000359211.3:n.150+2T>A
|
|
|
ENST00000460019.1:n.225+2T>A
|
|
|
|
NM_000110.3:c.150+2T>A , LRG_722t1:c.150+2T>A
|
NP_000101.2:n.150+2T>A
|
|
|
NM_001160301.1:c.150+2T>A , LRG_722t2:c.150+2T>A
|
NP_001153773.1:n.150+2T>A
|
|
|
XM_005270562.3:c.150+2T>A
|
XP_005270619.2:n.150+2T>A
|
|
|
XM_006710397.2:c.150+2T>A
|
XP_006710460.1:n.150+2T>A
|
|
|
XM_006710397.3:c.150+2T>A
|
XP_006710460.1:n.150+2T>A
|
|
|
XM_017000507.1:c.39+37622T>A
|
XP_016855996.1:n.39+37622T>A
|
|
|
XM_017000508.2:c.-561+2T>A
|
XP_016855997.1:n.-561+2T>A
|
|
|
XM_017000509.2:c.-459+2T>A
|
XP_016855998.1:n.-459+2T>A
|
|
|
XM_017000510.1:c.-459+37622T>A
|
XP_016855999.1:n.-459+37622T>A
|
|
|
XR_001737014.1:n.287+2T>A
|
|
|
|
NM_000110.4:c.150+2T>A
MANE Select
|
NP_000101.2:n.150+2T>A
|
|
