ENST00000534624.6:c.1341T>G
MANE Select
|
ENSP00000432083.1:p.Arg447=
|
|
ENST00000227378.7:c.1341T>G
|
ENSP00000227378.3:p.Arg447=
|
|
ENST00000453788.6:c.1341T>G
|
ENSP00000404372.2:p.Arg447=
|
|
ENST00000524552.5:c.114T>G
|
ENSP00000435908.1:p.Arg38=
|
|
ENST00000526110.5:c.1284T>G
|
ENSP00000433584.1:p.Arg428=
|
|
ENST00000526686.1:c.-4T>G
|
ENSP00000435019.1:n.-4T>G
|
|
ENST00000532091.1:n.1316T>G
|
|
|
ENST00000532636.5:c.1341T>G
|
ENSP00000437125.1:p.Arg447=
|
|
ENST00000533238.5:n.443T>G
|
|
|
ENST00000533540.5:c.903T>G
|
ENSP00000437189.1:p.Arg301=
|
|
ENST00000534319.5:c.633T>G
|
ENSP00000433316.1:p.Arg211=
|
|
ENST00000534624.5:c.1341T>G
|
ENSP00000432083.1:p.Arg447=
|
|
NM_006597.5:c.1341T>G
|
NP_006588.1:p.Arg447=
|
|
NM_153201.3:c.1341T>G
|
NP_694881.1:p.Arg447=
|
|
XM_011542798.1:c.1341T>G
|
XP_011541100.1:p.Arg447=
|
|
NM_006597.6:c.1341T>G
MANE Select
|
NP_006588.1:p.Arg447=
|
|
NM_153201.4:c.1341T>G
|
NP_694881.1:p.Arg447=
|
|