ENST00000306010.8:c.596T>G
|
ENSP00000302111.7:p.Leu199Arg
|
|
ENST00000651593.1:c.503T>G
MANE Select
|
ENSP00000498729.1:p.Leu168Arg
|
|
ENST00000306010.7:c.596T>G
|
ENSP00000302111.7:p.Leu199Arg
|
|
NM_002412.3:c.596T>G
|
NP_002403.2:p.Leu199Arg
|
|
NM_002412.4:c.596T>G
|
NP_002403.2:p.Leu199Arg
|
|
XM_005252682.2:c.503T>G
|
XP_005252739.1:p.Leu168Arg
|
|
XM_006717863.2:c.326T>G
|
XP_006717926.1:p.Leu109Arg
|
|
XM_011539817.1:c.512T>G
|
XP_011538119.1:p.Leu171Arg
|
|
NM_002412.5:c.503T>G
MANE Select
|
NP_002403.3:p.Leu168Arg
|
|
XM_017016275.1:c.326T>G
|
XP_016871764.1:p.Leu109Arg
|
|