ENST00000292408.9:c.2259+47G>T
MANE Select
|
ENSP00000292408.4:n.2259+47G>T
|
|
ENST00000292408.8:c.2259+47G>T
|
ENSP00000292408.4:n.2259+47G>T
|
|
ENST00000393637.5:c.2139+47G>T
|
ENSP00000377254.1:n.2139+47G>T
|
|
ENST00000393648.6:c.2055+47G>T
|
ENSP00000377259.2:n.2055+47G>T
|
|
ENST00000502906.5:c.2259+47G>T
|
ENSP00000424960.1:n.2259+47G>T
|
|
ENST00000513423.1:n.207+47G>T
|
|
|
NM_001291980.1:c.2055+47G>T
|
NP_001278909.1:n.2055+47G>T
|
|
NM_002011.4:c.2259+47G>T
|
NP_002002.3:n.2259+47G>T
|
|
NM_022963.3:c.2139+47G>T
|
NP_075252.2:n.2139+47G>T
|
|
NM_213647.2:c.2259+47G>T
|
NP_998812.1:n.2259+47G>T
|
|
XM_005265838.2:c.2259+47G>T
|
XP_005265895.1:n.2259+47G>T
|
|
XM_011534464.1:c.2352+47G>T
|
XP_011532766.1:n.2352+47G>T
|
|
XM_011534465.1:c.1941+47G>T
|
XP_011532767.1:n.1941+47G>T
|
|
NM_001354984.1:c.2259+47G>T
|
NP_001341913.1:n.2259+47G>T
|
|
NM_213647.3:c.2259+47G>T
MANE Select
|
NP_998812.1:n.2259+47G>T
|
|
NM_001291980.2:c.2055+47G>T
|
NP_001278909.1:n.2055+47G>T
|
|
NM_001354984.2:c.2259+47G>T
|
NP_001341913.1:n.2259+47G>T
|
|
NM_002011.5:c.2259+47G>T
|
NP_002002.3:n.2259+47G>T
|
|