ENST00000651671.1:c.1252C>T
MANE Select
|
ENSP00000498587.1:p.Leu418=
|
|
ENST00000679595.1:c.1252C>T
|
ENSP00000506241.1:p.Leu418=
|
|
ENST00000680133.1:c.1252C>T
|
ENSP00000505319.1:p.Leu418=
|
|
ENST00000680218.1:c.1252C>T
|
ENSP00000505339.1:p.Leu418=
|
|
ENST00000680668.1:c.1252C>T
|
ENSP00000506336.1:p.Leu418=
|
|
ENST00000680924.1:c.1252C>T
|
ENSP00000506031.1:p.Leu418=
|
|
ENST00000681135.1:c.1252C>T
|
ENSP00000506636.1:p.Leu418=
|
|
ENST00000681454.1:c.*488C>T
|
ENSP00000505763.1:n.*488C>T
|
|
ENST00000277541.6:c.1252C>T
|
ENSP00000277541.6:p.Leu418=
|
|
NM_017617.3:c.1252C>T
|
NP_060087.3:p.Leu418=
|
|
XM_011518717.1:c.553C>T
|
XP_011517019.1:p.Leu185=
|
|
NM_017617.5:c.1252C>T
MANE Select
|
NP_060087.3:p.Leu418=
|
|
XM_011518717.2:c.529C>T
|
XP_011517019.2:p.Leu177=
|
|