|
ENST00000257966.13:c.580-1491C>T
|
ENSP00000257966.8:n.580-1491C>T
|
|
|
ENST00000389142.10:c.580-1491C>T
|
ENSP00000373794.5:n.580-1491C>T
|
|
|
ENST00000389146.11:c.580-1491C>T
|
ENSP00000373798.6:n.580-1491C>T
|
|
|
ENST00000546916.2:n.901-1491C>T
|
|
|
|
ENST00000549897.2:n.1808-1491C>T
|
|
|
|
ENST00000550202.2:n.901-1491C>T
|
|
|
|
ENST00000550699.6:n.901-1491C>T
|
|
|
|
ENST00000552285.6:c.580-1491C>T
|
ENSP00000450010.1:n.580-1491C>T
|
|
|
ENST00000552423.2:c.*337-1491C>T
|
ENSP00000447163.1:n.*337-1491C>T
|
|
|
ENST00000553208.6:n.884-1491C>T
|
|
|
|
ENST00000700656.1:c.580-1491C>T
|
ENSP00000515125.1:n.580-1491C>T
|
|
|
ENST00000700657.1:c.580-1491C>T
|
ENSP00000515126.1:n.580-1491C>T
|
|
|
ENST00000700658.1:c.580-1491C>T
|
ENSP00000515127.1:n.580-1491C>T
|
|
|
ENST00000700659.1:c.580-1491C>T
|
ENSP00000515128.1:n.580-1491C>T
|
|
|
ENST00000700660.1:c.580-1491C>T
|
ENSP00000515129.1:n.580-1491C>T
|
|
|
ENST00000700661.1:c.580-1491C>T
|
ENSP00000515130.1:n.580-1491C>T
|
|
|
ENST00000700662.1:c.580-1491C>T
|
ENSP00000515131.1:n.580-1491C>T
|
|
|
ENST00000700663.1:c.580-1491C>T
|
ENSP00000515132.1:n.580-1491C>T
|
|
|
ENST00000700664.1:c.580-1491C>T
|
ENSP00000515133.1:n.580-1491C>T
|
|
|
ENST00000700665.1:c.580-1491C>T
|
ENSP00000515134.1:n.580-1491C>T
|
|
|
ENST00000700667.1:c.*383-1491C>T
|
ENSP00000515135.1:n.*383-1491C>T
|
|
|
ENST00000700668.1:c.268-1491C>T
|
ENSP00000515136.1:n.268-1491C>T
|
|
|
ENST00000315970.12:c.580-1491C>T
MANE Select
|
ENSP00000318165.7:n.580-1491C>T
|
|
|
ENST00000257966.12:c.580-1491C>T
|
ENSP00000257966.8:n.580-1491C>T
|
|
|
ENST00000315970.11:c.580-1491C>T
|
ENSP00000318165.7:n.580-1491C>T
|
|
|
ENST00000389142.9:c.580-1491C>T
|
ENSP00000373794.5:n.580-1491C>T
|
|
|
ENST00000389146.10:c.580-1491C>T
|
ENSP00000373798.6:n.580-1491C>T
|
|
|
ENST00000413095.6:c.404-2452C>T
|
ENSP00000413112.2:n.404-2452C>T
|
|
|
ENST00000435406.6:c.424-1491C>T
|
ENSP00000389632.2:n.424-1491C>T
|
|
|
ENST00000439210.6:c.403-1491C>T
|
ENSP00000407360.2:n.403-1491C>T
|
|
|
ENST00000547079.5:c.404-4067C>T
|
ENSP00000447031.1:n.404-4067C>T
|
|
|
ENST00000549307.5:n.761-1491C>T
|
|
|
|
ENST00000550372.5:c.400-1491C>T
|
ENSP00000447719.1:n.400-1491C>T
|
|
|
ENST00000551035.5:c.481-1491C>T
|
ENSP00000447866.1:n.481-1491C>T
|
|
|
ENST00000552285.5:c.580-1491C>T
|
ENSP00000450010.1:n.580-1491C>T
|
|
|
ENST00000552787.5:c.*77-1491C>T
|
ENSP00000447451.1:n.*77-1491C>T
|
|
|
ENST00000553208.5:n.831-1491C>T
|
|
|
|
NM_001017956.2:c.580-1491C>T
|
NP_001017956.1:n.580-1491C>T
|
|
|
NM_001017957.2:c.580-1491C>T
|
NP_001017957.1:n.580-1491C>T
|
|
|
NM_001017958.2:c.580-1491C>T
|
NP_001017958.1:n.580-1491C>T
|
|
|
NM_001261420.1:c.580-1491C>T
|
NP_001248349.1:n.580-1491C>T
|
|
|
NM_001261421.1:c.481-1491C>T
|
NP_001248350.1:n.481-1491C>T
|
|
|
NM_001261422.1:c.424-1491C>T
|
NP_001248351.1:n.424-1491C>T
|
|
|
NM_001261423.1:c.403-1491C>T
|
NP_001248352.1:n.403-1491C>T
|
|
|
NM_006812.3:c.580-1491C>T
|
NP_006803.1:n.580-1491C>T
|
|
|
XM_005268581.1:c.580-1491C>T
|
XP_005268638.1:n.580-1491C>T
|
|
|
XM_006719200.1:c.580-1491C>T
|
XP_006719263.1:n.580-1491C>T
|
|
|
XM_006719201.1:c.580-1491C>T
|
XP_006719264.1:n.580-1491C>T
|
|
|
XM_005268581.2:c.580-1491C>T
|
XP_005268638.1:n.580-1491C>T
|
|
|
XM_006719200.2:c.580-1491C>T
|
XP_006719263.1:n.580-1491C>T
|
|
|
XM_006719201.2:c.580-1491C>T
|
XP_006719264.1:n.580-1491C>T
|
|
|
NM_006812.4:c.580-1491C>T
MANE Select
|
NP_006803.1:n.580-1491C>T
|
|
|
NM_001017956.3:c.580-1491C>T
|
NP_001017956.1:n.580-1491C>T
|
|
|
NM_001017957.3:c.580-1491C>T
|
NP_001017957.1:n.580-1491C>T
|
|
|
NM_001017958.3:c.580-1491C>T
|
NP_001017958.1:n.580-1491C>T
|
|
|
NM_001261420.2:c.580-1491C>T
|
NP_001248349.1:n.580-1491C>T
|
|
|
NM_001261421.2:c.481-1491C>T
|
NP_001248350.1:n.481-1491C>T
|
|
|
NM_001261422.2:c.424-1491C>T
|
NP_001248351.1:n.424-1491C>T
|
|
|
NM_001261423.2:c.403-1491C>T
|
NP_001248352.1:n.403-1491C>T
|
|
