ENST00000524470.2:c.*1257+197G>T
|
ENSP00000514307.1:n.*1257+197G>T
|
|
ENST00000525976.6:c.2908+197G>T
|
ENSP00000434831.2:n.2908+197G>T
|
|
ENST00000527481.3:c.2908+197G>T
|
ENSP00000466340.2:n.2908+197G>T
|
|
ENST00000529370.6:n.4284+197G>T
|
|
|
ENST00000529739.2:n.3519G>T
|
|
|
ENST00000530829.2:c.*2459+197G>T
|
ENSP00000436826.2:n.*2459+197G>T
|
|
ENST00000531836.6:c.2908+197G>T
|
ENSP00000436175.2:n.2908+197G>T
|
|
ENST00000533334.2:c.*950+197G>T
|
ENSP00000432320.2:n.*950+197G>T
|
|
ENST00000534228.2:n.4564G>T
|
|
|
ENST00000699354.1:n.1010+197G>T
|
|
|
ENST00000699355.1:c.*2210G>T
|
ENSP00000514328.1:n.*2210G>T
|
|
ENST00000699356.1:n.3519G>T
|
|
|
ENST00000699357.1:n.4564G>T
|
|
|
ENST00000699358.1:c.2908+197G>T
|
ENSP00000514329.1:n.2908+197G>T
|
|
ENST00000699359.1:c.114+197G>T
|
|
|
ENST00000699360.1:c.2908+197G>T
|
ENSP00000514331.1:n.2908+197G>T
|
|
ENST00000699365.1:c.-55G>T
|
ENSP00000514334.1:n.-55G>T
|
|
ENST00000699366.1:n.80G>T
|
|
|
ENST00000699367.1:n.80G>T
|
|
|
ENST00000699368.1:c.197G>T
|
ENSP00000514335.1:n.197G>T
|
|
ENST00000525621.6:c.2908+197G>T
MANE Select
|
ENSP00000431885.1:n.2908+197G>T
|
|
ENST00000264818.10:c.2908+197G>T
|
ENSP00000264818.6:n.2908+197G>T
|
|
ENST00000524462.5:c.2353+197G>T
|
ENSP00000433203.1:n.2353+197G>T
|
|
ENST00000525621.5:c.2908+197G>T
|
ENSP00000431885.1:n.2908+197G>T
|
|
ENST00000527481.2:c.204+197G>T
|
|
|
ENST00000529739.1:c.-222G>T
|
ENSP00000436155.1:n.-222G>T
|
|
ENST00000530560.5:c.337+197G>T
|
ENSP00000465291.1:n.337+197G>T
|
|
ENST00000592137.1:n.62+197G>T
|
|
|
NM_003331.4:c.2908+197G>T , LRG_121t1:c.2908+197G>T
|
NP_003322.3:n.2908+197G>T
|
|
XM_011528245.1:c.2908+197G>T
|
XP_011526547.1:n.2908+197G>T
|
|
XM_011528246.1:c.2611+197G>T
|
XP_011526548.1:n.2611+197G>T
|
|
XM_011528247.1:c.2611+197G>T
|
XP_011526549.1:n.2611+197G>T
|
|
XM_011528248.1:c.2908+197G>T
|
XP_011526550.1:n.2908+197G>T
|
|
XM_011528249.1:c.1582+197G>T
|
XP_011526551.1:n.1582+197G>T
|
|
XM_011528251.1:c.1165+197G>T
|
XP_011526553.1:n.1165+197G>T
|
|
XM_011528246.3:c.2611+197G>T
|
XP_011526548.1:n.2611+197G>T
|
|
XM_011528249.2:c.1582+197G>T
|
XP_011526551.1:n.1582+197G>T
|
|
XR_001753750.1:n.3065+197G>T
|
|
|
XR_001753751.1:n.3262G>T
|
|
|
XR_002958353.1:n.4188G>T
|
|
|
NM_003331.5:c.2908+197G>T
MANE Select
|
NP_003322.3:n.2908+197G>T
|
|
NM_001385197.1:c.2908+197G>T
|
NP_001372126.1:n.2908+197G>T
|
|
NM_001385198.1:c.2908+197G>T
|
NP_001372127.1:n.2908+197G>T
|
|
NM_001385199.1:c.2722+197G>T
|
NP_001372128.1:n.2722+197G>T
|
|
NM_001385200.1:c.2905+197G>T
|
NP_001372129.1:n.2905+197G>T
|
|
NM_001385201.1:c.2710+197G>T
|
NP_001372130.1:n.2710+197G>T
|
|
NM_001385202.1:c.2824+197G>T
|
NP_001372131.1:n.2824+197G>T
|
|
NM_001385203.1:c.2989+197G>T
|
NP_001372132.1:n.2989+197G>T
|
|
NM_001385204.1:c.3118+197G>T
|
NP_001372133.1:n.3118+197G>T
|
|
NM_001385205.1:c.2818+197G>T
|
NP_001372134.1:n.2818+197G>T
|
|
NM_001385206.1:c.2782+197G>T
|
NP_001372135.1:n.2782+197G>T
|
|
NM_001385207.1:c.2890+197G>T
|
NP_001372136.1:n.2890+197G>T
|
|