ENST00000545399.6:c.755G>T
|
ENSP00000444688.1:p.Cys252Phe
|
|
ENST00000644613.1:c.716G>T
|
ENSP00000494711.1:p.Cys239Phe
|
|
ENST00000645448.1:n.948G>T
|
|
|
ENST00000648268.1:c.716G>T
MANE Select
|
ENSP00000498113.1:p.Cys239Phe
|
|
ENST00000302102.9:c.716G>T
|
ENSP00000302397.5:p.Cys239Phe
|
|
ENST00000441343.5:c.716G>T
|
ENSP00000411503.1:p.Cys239Phe
|
|
ENST00000473086.3:c.626G>T
|
ENSP00000469129.2:p.Cys209Phe
|
|
ENST00000485672.2:n.29G>T
|
|
|
ENST00000543770.5:c.749G>T
|
ENSP00000437577.1:p.Cys250Phe
|
|
ENST00000545399.5:c.755G>T
|
ENSP00000444688.1:p.Cys252Phe
|
|
ENST00000602133.5:c.626G>T
|
ENSP00000471581.1:p.Cys209Phe
|
|
NM_001256213.1:c.749G>T
|
NP_001243142.1:p.Cys250Phe
|
|
NM_001256214.1:c.755G>T
|
NP_001243143.1:p.Cys252Phe
|
|
NM_152296.4:c.716G>T
|
NP_689509.1:p.Cys239Phe
|
|
XM_011526991.1:c.626G>T
|
XP_011525293.1:p.Cys209Phe
|
|
NM_152296.5:c.716G>T
MANE Select
|
NP_689509.1:p.Cys239Phe
|
|
NM_001256214.2:c.755G>T
|
NP_001243143.1:p.Cys252Phe
|
|
NM_001256213.2:c.749G>T
|
NP_001243142.1:p.Cys250Phe
|
|