ENST00000432588.6:c.567C>T
|
ENSP00000407473.2:p.Leu189=
|
|
ENST00000473257.3:c.438C>T
|
ENSP00000501773.1:p.Leu146=
|
|
ENST00000477812.2:n.1114C>T
|
|
|
ENST00000493945.6:c.567C>T
|
ENSP00000494269.1:p.Leu189=
|
|
ENST00000642480.2:c.567C>T
|
ENSP00000495995.2:p.Leu189=
|
|
ENST00000645576.1:c.519C>T
|
ENSP00000496101.1:p.Leu173=
|
|
ENST00000646664.1:c.567C>T
MANE Select
|
ENSP00000494750.1:p.Leu189=
|
|
ENST00000647275.1:c.201C>T
|
ENSP00000494185.1:p.Leu67=
|
|
ENST00000674681.1:c.567C>T
|
ENSP00000502821.1:p.Leu189=
|
|
ENST00000675515.1:c.567C>T
|
ENSP00000501862.1:p.Leu189=
|
|
ENST00000676189.1:c.*110C>T
|
ENSP00000502538.1:n.*110C>T
|
|
ENST00000676319.1:c.88-733C>T
|
ENSP00000502193.1:n.88-733C>T
|
|
ENST00000676397.1:c.567C>T
|
ENSP00000502286.1:p.Leu189=
|
|
ENST00000331789.9:c.567C>T
|
ENSP00000349960.4:p.Leu189=
|
|
ENST00000425660.5:c.*230C>T
|
ENSP00000409264.1:n.*230C>T
|
|
ENST00000462494.5:n.1092C>T
|
|
|
ENST00000473257.1:n.285C>T
|
|
|
ENST00000477812.1:n.774C>T
|
|
|
ENST00000484841.5:n.722C>T
|
|
|
ENST00000493945.5:n.573C>T
|
|
|
NM_001101.3:c.567C>T , LRG_132t1:c.567C>T
|
NP_001092.1:p.Leu189=
|
|
XM_006715764.1:c.201C>T
|
XP_006715827.1:p.Leu67=
|
|
NM_001101.4:c.567C>T
|
NP_001092.1:p.Leu189=
|
|
NM_001101.5:c.567C>T
MANE Select
|
NP_001092.1:p.Leu189=
|
|