ENST00000645828.1:n.2790G>A
|
|
|
ENST00000651671.1:c.4983G>A
MANE Select
|
ENSP00000498587.1:p.Arg1661=
|
|
ENST00000679595.1:c.4983G>A
|
ENSP00000506241.1:p.Arg1661=
|
|
ENST00000680133.1:c.4869G>A
|
ENSP00000505319.1:p.Arg1623=
|
|
ENST00000680218.1:c.4863G>A
|
ENSP00000505339.1:p.Arg1621=
|
|
ENST00000680668.1:c.4869G>A
|
ENSP00000506336.1:p.Arg1623=
|
|
ENST00000680778.1:c.2580G>A
|
ENSP00000506033.1:p.Arg860=
|
|
ENST00000680924.1:c.*2383G>A
|
ENSP00000506031.1:n.*2383G>A
|
|
ENST00000681135.1:c.*2592G>A
|
ENSP00000506636.1:n.*2592G>A
|
|
ENST00000681298.1:n.1796G>A
|
|
|
ENST00000681454.1:c.*4219G>A
|
ENSP00000505763.1:n.*4219G>A
|
|
ENST00000277541.6:c.4983G>A
|
ENSP00000277541.6:p.Arg1661=
|
|
ENST00000494783.1:n.138G>A
|
|
|
NM_017617.3:c.4983G>A
|
NP_060087.3:p.Arg1661=
|
|
XM_011518717.1:c.4284G>A
|
XP_011517019.1:p.Arg1428=
|
|
NM_017617.5:c.4983G>A
MANE Select
|
NP_060087.3:p.Arg1661=
|
|
XM_011518717.2:c.4260G>A
|
XP_011517019.2:p.Arg1420=
|
|