ENST00000295754.10:c.1550T>A
MANE Select
|
ENSP00000295754.5:p.Leu517Ter
|
|
ENST00000672050.1:n.434T>A
|
|
|
ENST00000672866.1:n.3146T>A
|
|
|
ENST00000673203.1:n.428T>A
|
|
|
ENST00000295754.9:c.1550T>A
|
ENSP00000295754.5:p.Leu517Ter
|
|
ENST00000359013.4:c.1625T>A
|
ENSP00000351905.4:p.Leu542Ter
|
|
NM_001024847.2:c.1625T>A , LRG_779t1:c.1625T>A
|
NP_001020018.1:p.Leu542Ter
|
|
NM_003242.5:c.1550T>A
|
NP_003233.4:p.Leu517Ter
|
|
XM_011534043.1:c.1577T>A
|
XP_011532345.1:p.Leu526Ter
|
|
XM_011534044.1:c.1502T>A
|
XP_011532346.1:p.Leu501Ter
|
|
XM_011534045.1:c.1445T>A
|
XP_011532347.1:p.Leu482Ter
|
|
XM_011534043.2:c.1577T>A
|
XP_011532345.1:p.Leu526Ter
|
|
XM_011534045.3:c.1445T>A
|
XP_011532347.1:p.Leu482Ter
|
|
XM_017007106.1:c.1445T>A
|
XP_016862595.1:p.Leu482Ter
|
|
NM_003242.6:c.1550T>A
MANE Select
|
NP_003233.4:p.Leu517Ter
|
|