ENST00000696177.1:c.558T>G
|
ENSP00000512467.1:p.Ser186=
|
|
ENST00000696178.1:c.558T>G
|
ENSP00000512468.1:p.Ser186=
|
|
ENST00000696179.1:c.558T>G
|
ENSP00000512469.1:p.Ser186=
|
|
ENST00000696180.1:c.558T>G
|
ENSP00000512470.1:p.Ser186=
|
|
ENST00000696181.1:c.558T>G
|
ENSP00000512471.1:p.Ser186=
|
|
ENST00000696182.1:c.-114-14606T>G
|
ENSP00000512472.1:n.-114-14606T>G
|
|
ENST00000696184.1:c.558T>G
|
ENSP00000512473.1:p.Ser186=
|
|
ENST00000696185.1:n.1191T>G
|
|
|
ENST00000696186.1:c.558T>G
|
ENSP00000512474.1:p.Ser186=
|
|
ENST00000220562.9:c.558T>G
MANE Select
|
ENSP00000220562.4:p.Ser186=
|
|
ENST00000220562.8:c.558T>G
|
ENSP00000220562.4:p.Ser186=
|
|
ENST00000519886.5:n.631+551T>G
|
|
|
ENST00000521532.5:c.42+6114T>G
|
ENSP00000431013.1:n.42+6114T>G
|
|
ENST00000523149.5:c.28-622T>G
|
ENSP00000428691.1:n.28-622T>G
|
|
NM_001440.3:c.558T>G
|
NP_001431.1:p.Ser186=
|
|
NR_073468.1:n.188-14606T>G
|
|
|
NR_073469.1:n.763+551T>G
|
|
|
XM_011544440.1:c.558T>G
|
XP_011542742.1:p.Ser186=
|
|
XM_011544440.3:c.558T>G
|
XP_011542742.1:p.Ser186=
|
|
XM_024447094.1:c.558T>G
|
XP_024302862.1:p.Ser186=
|
|
XM_024447095.1:c.558T>G
|
XP_024302863.1:p.Ser186=
|
|
XM_024447096.1:c.558T>G
|
XP_024302864.1:p.Ser186=
|
|
NM_001440.4:c.558T>G
MANE Select
|
NP_001431.1:p.Ser186=
|
|
NR_073468.2:n.160-14606T>G
|
|
|
NR_073469.2:n.735+551T>G
|
|
|