ENST00000324071.10:c.1068T>A
MANE Select
|
ENSP00000324648.2:p.Ile356=
|
|
ENST00000598834.2:c.1092T>A
|
|
|
ENST00000324071.8:c.1068T>A
|
ENSP00000324648.2:p.Ile356=
|
|
ENST00000593831.1:c.360T>A
|
ENSP00000470582.1:p.Ile120=
|
|
ENST00000597612.1:n.563T>A
|
|
|
NM_000767.4:c.1068T>A
|
NP_000758.1:p.Ile356=
|
|
XM_005258569.3:c.1068T>A
|
XP_005258626.1:p.Ile356=
|
|
XM_006723050.2:c.1068T>A
|
XP_006723113.1:p.Ile356=
|
|
XM_011526546.1:c.1068T>A
|
XP_011524848.1:p.Ile356=
|
|
XM_011526547.1:c.1068T>A
|
XP_011524849.1:p.Ile356=
|
|
XM_011526548.1:c.588T>A
|
XP_011524850.1:p.Ile196=
|
|
XM_011526549.1:c.477T>A
|
XP_011524851.1:p.Ile159=
|
|
XM_011526550.1:c.468T>A
|
XP_011524852.1:p.Ile156=
|
|
NM_000767.5:c.1068T>A
MANE Select
|
NP_000758.1:p.Ile356=
|
|