ENST00000297784.10:c.1935C>T
MANE Select
|
ENSP00000297784.6:p.Phe645=
|
|
ENST00000644967.1:c.*375C>T
|
ENSP00000496159.1:n.*375C>T
|
|
ENST00000645053.1:c.1258-5856C>T
|
ENSP00000493838.1:n.1258-5856C>T
|
|
ENST00000645208.2:c.1935C>T
|
ENSP00000494684.1:p.Phe645=
|
|
ENST00000645773.1:c.1809C>T
|
ENSP00000493698.1:p.Phe603=
|
|
ENST00000645787.1:n.2078C>T
|
|
|
ENST00000646619.1:c.1497C>T
|
ENSP00000493726.1:p.Phe499=
|
|
ENST00000651183.1:c.1497C>T
|
ENSP00000498723.1:p.Phe499=
|
|
ENST00000297784.9:c.1935C>T
|
ENSP00000297784.5:p.Phe645=
|
|
ENST00000340019.4:c.1935C>T
|
ENSP00000341433.3:p.Phe645=
|
|
ENST00000469455.1:n.416C>T
|
|
|
ENST00000486417.5:n.833C>T
|
|
|
NM_138691.2:c.1935C>T
|
NP_619636.2:p.Phe645=
|
|
XM_011518213.1:c.2523C>T
|
XP_011516515.1:p.Phe841=
|
|
XM_017014256.1:c.1938C>T
|
XP_016869745.1:p.Phe646=
|
|
NM_138691.3:c.1935C>T
MANE Select
|
NP_619636.2:p.Phe645=
|
|