ENST00000371974.8:c.653_655delinsCTG
MANE Select
|
ENSP00000361042.3:p.Pro218=
|
|
ENST00000371974.7:c.653_655delinsCTG
|
ENSP00000361042.3:p.Pro218=
|
|
ENST00000437995.1:n.563_565delinsCTG
|
|
|
ENST00000495952.5:n.643_645delinsCTG
|
|
|
ENST00000615505.4:c.326_328delinsCTG
|
ENSP00000482067.1:p.Pro109=
|
|
NM_001280787.1:c.326_328delinsCTG
|
NP_001267716.1:p.Pro109=
|
|
NM_003172.3:c.653_655delinsCTG
|
NP_003163.1:p.Pro218=
|
|
XM_011518942.1:c.326_328delinsCTG
|
XP_011517244.1:p.Pro109=
|
|
NM_003172.4:c.653_655delinsCTG
MANE Select
|
NP_003163.1:p.Pro218=
|
|