ENST00000344922.10:c.4709+145T>C
MANE Select
|
ENSP00000340900.5:n.4709+145T>C
|
|
ENST00000340535.11:c.1343+145T>C
|
ENSP00000345866.7:n.1343+145T>C
|
|
ENST00000344507.1:c.1475-6631T>C
|
ENSP00000341348.1:n.1475-6631T>C
|
|
ENST00000344922.9:c.4709+145T>C
|
ENSP00000340900.5:n.4709+145T>C
|
|
ENST00000476400.1:n.182+145T>C
|
|
|
NM_001300867.1:c.1343+145T>C
|
NP_001287796.1:n.1343+145T>C
|
|
NM_198551.3:c.4709+145T>C
|
NP_940953.2:n.4709+145T>C
|
|
XM_005273121.3:c.4709+145T>C
|
XP_005273178.1:n.4709+145T>C
|
|
XM_006711304.2:c.4532+145T>C
|
XP_006711367.1:n.4532+145T>C
|
|
NM_001324062.1:c.4709+145T>C
|
NP_001310991.1:n.4709+145T>C
|
|
NM_001324063.1:c.4532+145T>C
|
NP_001310992.1:n.4532+145T>C
|
|
NM_001324064.1:c.4217+145T>C
|
NP_001310993.1:n.4217+145T>C
|
|
NM_001324065.1:c.1343+145T>C
|
NP_001310994.1:n.1343+145T>C
|
|
XM_006711304.4:c.4532+145T>C
|
XP_006711367.3:n.4532+145T>C
|
|
XM_017001243.2:c.4217+145T>C
|
XP_016856732.1:n.4217+145T>C
|
|
NM_198551.4:c.4709+145T>C
MANE Select
|
NP_940953.2:n.4709+145T>C
|
|
NM_001300867.2:c.1343+145T>C
|
NP_001287796.1:n.1343+145T>C
|
|
NM_001324062.2:c.4709+145T>C
|
NP_001310991.1:n.4709+145T>C
|
|
NM_001324063.2:c.4532+145T>C
|
NP_001310992.1:n.4532+145T>C
|
|
NM_001324064.2:c.4217+145T>C
|
NP_001310993.1:n.4217+145T>C
|
|
NM_001324065.2:c.1343+145T>C
|
NP_001310994.1:n.1343+145T>C
|
|