ENST00000651671.1:c.6114G>T
MANE Select
|
ENSP00000498587.1:p.Val2038=
|
|
ENST00000679595.1:c.*1154G>T
|
ENSP00000506241.1:n.*1154G>T
|
|
ENST00000679969.1:n.2710G>T
|
|
|
ENST00000680003.1:n.2446G>T
|
|
|
ENST00000680133.1:c.6000G>T
|
ENSP00000505319.1:p.Val2000=
|
|
ENST00000680218.1:c.5994G>T
|
ENSP00000505339.1:p.Val1998=
|
|
ENST00000680668.1:c.6000G>T
|
ENSP00000506336.1:p.Val2000=
|
|
ENST00000680778.1:c.3711G>T
|
ENSP00000506033.1:p.Val1237=
|
|
ENST00000680924.1:c.*3514G>T
|
ENSP00000506031.1:n.*3514G>T
|
|
ENST00000681135.1:c.*3723G>T
|
ENSP00000506636.1:n.*3723G>T
|
|
ENST00000681298.1:n.4219G>T
|
|
|
ENST00000681454.1:c.*5350G>T
|
ENSP00000505763.1:n.*5350G>T
|
|
ENST00000277541.6:c.6114G>T
|
ENSP00000277541.6:p.Val2038=
|
|
NM_017617.3:c.6114G>T
|
NP_060087.3:p.Val2038=
|
|
XM_011518717.1:c.5415G>T
|
XP_011517019.1:p.Val1805=
|
|
NM_017617.5:c.6114G>T
MANE Select
|
NP_060087.3:p.Val2038=
|
|
XM_011518717.2:c.5391G>T
|
XP_011517019.2:p.Val1797=
|
|