ENST00000651671.1:c.6033G>C
MANE Select
|
ENSP00000498587.1:p.Leu2011=
|
|
ENST00000679595.1:c.*1073G>C
|
ENSP00000506241.1:n.*1073G>C
|
|
ENST00000679969.1:n.2514G>C
|
|
|
ENST00000680003.1:n.2365G>C
|
|
|
ENST00000680133.1:c.5919G>C
|
ENSP00000505319.1:p.Leu1973=
|
|
ENST00000680218.1:c.5913G>C
|
ENSP00000505339.1:p.Leu1971=
|
|
ENST00000680668.1:c.5919G>C
|
ENSP00000506336.1:p.Leu1973=
|
|
ENST00000680778.1:c.3630G>C
|
ENSP00000506033.1:p.Leu1210=
|
|
ENST00000680924.1:c.*3433G>C
|
ENSP00000506031.1:n.*3433G>C
|
|
ENST00000681135.1:c.*3642G>C
|
ENSP00000506636.1:n.*3642G>C
|
|
ENST00000681298.1:n.4138G>C
|
|
|
ENST00000681454.1:c.*5269G>C
|
ENSP00000505763.1:n.*5269G>C
|
|
ENST00000277541.6:c.6033G>C
|
ENSP00000277541.6:p.Leu2011=
|
|
NM_017617.3:c.6033G>C
|
NP_060087.3:p.Leu2011=
|
|
XM_011518717.1:c.5334G>C
|
XP_011517019.1:p.Leu1778=
|
|
NM_017617.5:c.6033G>C
MANE Select
|
NP_060087.3:p.Leu2011=
|
|
XM_011518717.2:c.5310G>C
|
XP_011517019.2:p.Leu1770=
|
|