ENST00000325455.10:c.2357+457G>T
MANE Select
|
ENSP00000325120.5:n.2357+457G>T
|
|
ENST00000263463.9:c.2051+457G>T
|
ENSP00000263463.5:n.2051+457G>T
|
|
ENST00000325455.9:c.2357+457G>T
|
ENSP00000325120.5:n.2357+457G>T
|
|
ENST00000526300.5:c.2051+457G>T
|
ENSP00000436803.1:n.2051+457G>T
|
|
ENST00000528960.5:c.2240+457G>T
|
ENSP00000432914.1:n.2240+457G>T
|
|
ENST00000530764.1:n.47+457G>T
|
|
|
ENST00000533207.5:n.1724+457G>T
|
|
|
ENST00000534013.5:c.575+457G>T
|
ENSP00000436561.1:n.575+457G>T
|
|
ENST00000534780.5:c.2357+457G>T
|
ENSP00000432352.1:n.2357+457G>T
|
|
ENST00000617858.4:c.2052-18G>T
|
ENSP00000481227.1:n.2052-18G>T
|
|
ENST00000619228.2:c.2240+457G>T
|
ENSP00000482698.1:n.2240+457G>T
|
|
NM_000926.4:c.2357+457G>T
MANE Select
|
NP_000917.3:n.2357+457G>T
|
|
NM_001202474.3:c.1865+457G>T
|
NP_001189403.1:n.1865+457G>T
|
|
NM_001271161.2:c.1559+457G>T
|
NP_001258090.1:n.1559+457G>T
|
|
NM_001271162.1:c.575+457G>T
|
NP_001258091.1:n.575+457G>T
|
|
NR_073141.2:n.2350+457G>T
|
|
|
NR_073142.2:n.2233+457G>T
|
|
|
NR_073143.2:n.2044+457G>T
|
|
|
XM_006718858.2:c.2357+457G>T
|
XP_006718921.1:n.2357+457G>T
|
|
XM_006718858.3:c.2357+457G>T
|
XP_006718921.1:n.2357+457G>T
|
|
NM_001271162.2:c.575+457G>T
|
NP_001258091.1:n.575+457G>T
|
|
NR_073141.3:n.2364+457G>T
|
|
|
NR_073142.3:n.2247+457G>T
|
|
|
NR_073143.3:n.2058+457G>T
|
|
|