ENST00000534624.6:c.1242C>T
MANE Select
|
ENSP00000432083.1:p.Ile414=
|
|
ENST00000227378.7:c.1242C>T
|
ENSP00000227378.3:p.Ile414=
|
|
ENST00000453788.6:c.1242C>T
|
ENSP00000404372.2:p.Ile414=
|
|
ENST00000524552.5:c.15C>T
|
ENSP00000435908.1:p.Ile5=
|
|
ENST00000526110.5:c.1185C>T
|
ENSP00000433584.1:p.Ile395=
|
|
ENST00000532091.1:n.989C>T
|
|
|
ENST00000532636.5:c.1242C>T
|
ENSP00000437125.1:p.Ile414=
|
|
ENST00000533238.5:n.381-37C>T
|
|
|
ENST00000533540.5:c.804C>T
|
ENSP00000437189.1:p.Ile268=
|
|
ENST00000534319.5:c.534C>T
|
ENSP00000433316.1:p.Ile178=
|
|
ENST00000534624.5:c.1242C>T
|
ENSP00000432083.1:p.Ile414=
|
|
NM_006597.5:c.1242C>T
|
NP_006588.1:p.Ile414=
|
|
NM_153201.3:c.1242C>T
|
NP_694881.1:p.Ile414=
|
|
XM_011542798.1:c.1242C>T
|
XP_011541100.1:p.Ile414=
|
|
NM_006597.6:c.1242C>T
MANE Select
|
NP_006588.1:p.Ile414=
|
|
NM_153201.4:c.1242C>T
|
NP_694881.1:p.Ile414=
|
|