ENST00000645828.1:n.2688C>G
|
|
|
ENST00000651671.1:c.4881C>G
MANE Select
|
ENSP00000498587.1:p.Arg1627=
|
|
ENST00000679595.1:c.4881C>G
|
ENSP00000506241.1:p.Arg1627=
|
|
ENST00000680133.1:c.4767C>G
|
ENSP00000505319.1:p.Arg1589=
|
|
ENST00000680218.1:c.4761C>G
|
ENSP00000505339.1:p.Arg1587=
|
|
ENST00000680668.1:c.4767C>G
|
ENSP00000506336.1:p.Arg1589=
|
|
ENST00000680778.1:c.2478C>G
|
ENSP00000506033.1:p.Arg826=
|
|
ENST00000680924.1:c.*2281C>G
|
ENSP00000506031.1:n.*2281C>G
|
|
ENST00000681135.1:c.*2490C>G
|
ENSP00000506636.1:n.*2490C>G
|
|
ENST00000681298.1:n.1694C>G
|
|
|
ENST00000681454.1:c.*4117C>G
|
ENSP00000505763.1:n.*4117C>G
|
|
ENST00000277541.6:c.4881C>G
|
ENSP00000277541.6:p.Arg1627=
|
|
ENST00000494783.1:n.36C>G
|
|
|
NM_017617.3:c.4881C>G
|
NP_060087.3:p.Arg1627=
|
|
XM_011518717.1:c.4182C>G
|
XP_011517019.1:p.Arg1394=
|
|
NM_017617.5:c.4881C>G
MANE Select
|
NP_060087.3:p.Arg1627=
|
|
XM_011518717.2:c.4158C>G
|
XP_011517019.2:p.Arg1386=
|
|