ENST00000696177.1:c.732G>T
|
ENSP00000512467.1:p.Glu244Asp
|
|
ENST00000696178.1:c.732G>T
|
ENSP00000512468.1:p.Glu244Asp
|
|
ENST00000696179.1:c.732G>T
|
ENSP00000512469.1:p.Glu244Asp
|
|
ENST00000696180.1:c.732G>T
|
ENSP00000512470.1:p.Glu244Asp
|
|
ENST00000696181.1:c.732G>T
|
ENSP00000512471.1:p.Glu244Asp
|
|
ENST00000696182.1:c.-114-14432G>T
|
ENSP00000512472.1:n.-114-14432G>T
|
|
ENST00000696184.1:c.732G>T
|
ENSP00000512473.1:p.Glu244Asp
|
|
ENST00000696185.1:n.1365G>T
|
|
|
ENST00000696186.1:c.732G>T
|
ENSP00000512474.1:p.Glu244Asp
|
|
ENST00000220562.9:c.732G>T
MANE Select
|
ENSP00000220562.4:p.Glu244Asp
|
|
ENST00000220562.8:c.732G>T
|
ENSP00000220562.4:p.Glu244Asp
|
|
ENST00000519886.5:n.631+725G>T
|
|
|
ENST00000521532.5:c.42+6288G>T
|
ENSP00000431013.1:n.42+6288G>T
|
|
ENST00000522698.1:c.107G>T
|
|
|
ENST00000523149.5:c.28-448G>T
|
ENSP00000428691.1:n.28-448G>T
|
|
NM_001440.3:c.732G>T
|
NP_001431.1:p.Glu244Asp
|
|
NR_073468.1:n.188-14432G>T
|
|
|
NR_073469.1:n.763+725G>T
|
|
|
XM_011544440.1:c.732G>T
|
XP_011542742.1:p.Glu244Asp
|
|
XM_011544440.3:c.732G>T
|
XP_011542742.1:p.Glu244Asp
|
|
XM_024447094.1:c.732G>T
|
XP_024302862.1:p.Glu244Asp
|
|
XM_024447095.1:c.732G>T
|
XP_024302863.1:p.Glu244Asp
|
|
XM_024447096.1:c.732G>T
|
XP_024302864.1:p.Glu244Asp
|
|
NM_001440.4:c.732G>T
MANE Select
|
NP_001431.1:p.Glu244Asp
|
|
NR_073468.2:n.160-14432G>T
|
|
|
NR_073469.2:n.735+725G>T
|
|
|