ENST00000651671.1:c.6081G>C
MANE Select
|
ENSP00000498587.1:p.Leu2027=
|
|
ENST00000679595.1:c.*1121G>C
|
ENSP00000506241.1:n.*1121G>C
|
|
ENST00000679969.1:n.2562G>C
|
|
|
ENST00000680003.1:n.2413G>C
|
|
|
ENST00000680133.1:c.5967G>C
|
ENSP00000505319.1:p.Leu1989=
|
|
ENST00000680218.1:c.5961G>C
|
ENSP00000505339.1:p.Leu1987=
|
|
ENST00000680668.1:c.5967G>C
|
ENSP00000506336.1:p.Leu1989=
|
|
ENST00000680778.1:c.3678G>C
|
ENSP00000506033.1:p.Leu1226=
|
|
ENST00000680924.1:c.*3481G>C
|
ENSP00000506031.1:n.*3481G>C
|
|
ENST00000681135.1:c.*3690G>C
|
ENSP00000506636.1:n.*3690G>C
|
|
ENST00000681298.1:n.4186G>C
|
|
|
ENST00000681454.1:c.*5317G>C
|
ENSP00000505763.1:n.*5317G>C
|
|
ENST00000277541.6:c.6081G>C
|
ENSP00000277541.6:p.Leu2027=
|
|
NM_017617.3:c.6081G>C
|
NP_060087.3:p.Leu2027=
|
|
XM_011518717.1:c.5382G>C
|
XP_011517019.1:p.Leu1794=
|
|
NM_017617.5:c.6081G>C
MANE Select
|
NP_060087.3:p.Leu2027=
|
|
XM_011518717.2:c.5358G>C
|
XP_011517019.2:p.Leu1786=
|
|