ENST00000534624.6:c.1164T>G
MANE Select
|
ENSP00000432083.1:p.Val388=
|
|
ENST00000227378.7:c.1164T>G
|
ENSP00000227378.3:p.Val388=
|
|
ENST00000453788.6:c.1164T>G
|
ENSP00000404372.2:p.Val388=
|
|
ENST00000524552.5:c.-64T>G
|
ENSP00000435908.1:n.-64T>G
|
|
ENST00000526110.5:c.1107T>G
|
ENSP00000433584.1:p.Val369=
|
|
ENST00000526862.1:n.442T>G
|
|
|
ENST00000532091.1:n.911T>G
|
|
|
ENST00000532636.5:c.1164T>G
|
ENSP00000437125.1:p.Val388=
|
|
ENST00000533238.5:n.381-115T>G
|
|
|
ENST00000533540.5:c.726T>G
|
ENSP00000437189.1:p.Val242=
|
|
ENST00000534319.5:c.456T>G
|
ENSP00000433316.1:p.Val152=
|
|
ENST00000534624.5:c.1164T>G
|
ENSP00000432083.1:p.Val388=
|
|
NM_006597.5:c.1164T>G
|
NP_006588.1:p.Val388=
|
|
NM_153201.3:c.1164T>G
|
NP_694881.1:p.Val388=
|
|
XM_011542798.1:c.1164T>G
|
XP_011541100.1:p.Val388=
|
|
NM_006597.6:c.1164T>G
MANE Select
|
NP_006588.1:p.Val388=
|
|
NM_153201.4:c.1164T>G
|
NP_694881.1:p.Val388=
|
|