ENST00000306010.8:c.579G=
|
ENSP00000302111.7:p.Leu193=
|
|
ENST00000651593.1:c.486G=
MANE Select
|
ENSP00000498729.1:p.Leu162=
|
|
ENST00000306010.7:c.579G=
|
ENSP00000302111.7:p.Leu193=
|
|
NM_002412.3:c.579G=
|
NP_002403.2:p.Leu193=
|
|
NM_002412.4:c.579G=
|
NP_002403.2:p.Leu193=
|
|
XM_005252682.2:c.486G=
|
XP_005252739.1:p.Leu162=
|
|
XM_006717863.2:c.309G=
|
XP_006717926.1:p.Leu103=
|
|
XM_011539817.1:c.495G=
|
XP_011538119.1:p.Leu165=
|
|
NM_002412.5:c.486G=
MANE Select
|
NP_002403.3:p.Leu162=
|
|
XM_017016275.1:c.309G=
|
XP_016871764.1:p.Leu103=
|
|