ENST00000322048.12:c.654C>A
MANE Select
|
ENSP00000322832.6:p.Arg218=
|
|
ENST00000322048.11:c.654C>A
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ENSP00000322832.5:p.Arg218=
|
|
ENST00000586153.1:c.300C>A
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ENSP00000464699.1:p.Arg100=
|
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ENST00000586336.5:n.753C>A
|
|
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ENST00000586504.5:c.425+92C>A
|
|
|
ENST00000587377.5:c.667C>A
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ENSP00000468343.1:p.Pro223Thr
|
|
ENST00000587711.5:c.339C>A
|
ENSP00000467459.1:p.Arg113=
|
|
ENST00000587843.5:c.*392C>A
|
ENSP00000465970.1:n.*392C>A
|
|
ENST00000588201.5:c.*645C>A
|
ENSP00000466529.1:n.*645C>A
|
|
ENST00000589543.5:n.611C>A
|
|
|
ENST00000591292.5:n.1983C>A
|
|
|
ENST00000591392.5:c.582C>A
|
ENSP00000467509.1:p.Arg194=
|
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ENST00000592019.1:c.77-164C>A
|
|
|
NM_024589.2:c.654C>A , LRG_455t1:c.654C>A
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NP_078865.1:p.Arg218=
|
|
NR_046480.1:n.978C>A
|
|
|
XM_006720947.2:c.654C>A
|
XP_006721010.1:p.Arg218=
|
|
XM_006720948.2:c.384C>A
|
XP_006721011.1:p.Arg128=
|
|
XM_006720947.4:c.654C>A
|
XP_006721010.1:p.Arg218=
|
|
XM_006720948.4:c.384C>A
|
XP_006721011.1:p.Arg128=
|
|
NM_024589.3:c.654C>A
MANE Select
|
NP_078865.1:p.Arg218=
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|
NR_046480.2:n.661C>A
|
|
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