ENST00000322048.12:c.645+1G>T
MANE Select
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ENSP00000322832.6:n.645+1G>T
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ENST00000322048.11:c.645+1G>T
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ENSP00000322832.5:n.645+1G>T
|
|
ENST00000586153.1:c.291+1G>T
|
ENSP00000464699.1:n.291+1G>T
|
|
ENST00000586336.5:n.744+1G>T
|
|
|
ENST00000586504.5:c.425+1G>T
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|
|
ENST00000587377.5:c.658+1G>T
|
ENSP00000468343.1:n.658+1G>T
|
|
ENST00000587711.5:c.330+1G>T
|
ENSP00000467459.1:n.330+1G>T
|
|
ENST00000587843.5:c.*383+1G>T
|
ENSP00000465970.1:n.*383+1G>T
|
|
ENST00000588201.5:c.*636+1G>T
|
ENSP00000466529.1:n.*636+1G>T
|
|
ENST00000589543.5:n.602+1G>T
|
|
|
ENST00000591292.5:n.1974+1G>T
|
|
|
ENST00000591392.5:c.573+1G>T
|
ENSP00000467509.1:n.573+1G>T
|
|
ENST00000592019.1:c.77-255G>T
|
|
|
NM_024589.2:c.645+1G>T , LRG_455t1:c.645+1G>T
|
NP_078865.1:n.645+1G>T
|
|
NR_046480.1:n.969+1G>T
|
|
|
XM_006720947.2:c.645+1G>T
|
XP_006721010.1:n.645+1G>T
|
|
XM_006720948.2:c.375+1G>T
|
XP_006721011.1:n.375+1G>T
|
|
XM_006720947.4:c.645+1G>T
|
XP_006721010.1:n.645+1G>T
|
|
XM_006720948.4:c.375+1G>T
|
XP_006721011.1:n.375+1G>T
|
|
NM_024589.3:c.645+1G>T
MANE Select
|
NP_078865.1:n.645+1G>T
|
|
NR_046480.2:n.652+1G>T
|
|
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