ENST00000324071.10:c.486G>T
MANE Select
|
ENSP00000324648.2:p.Gly162=
|
|
ENST00000598834.2:c.388G>T
|
|
|
ENST00000324071.8:c.486G>T
|
ENSP00000324648.2:p.Gly162=
|
|
ENST00000593831.1:c.256+2460G>T
|
ENSP00000470582.1:n.256+2460G>T
|
|
ENST00000594187.1:n.70G>T
|
|
|
ENST00000598834.1:n.388G>T
|
|
|
NM_000767.4:c.486G>T
|
NP_000758.1:p.Gly162=
|
|
XM_005258569.3:c.486G>T
|
XP_005258626.1:p.Gly162=
|
|
XM_006723050.2:c.486G>T
|
XP_006723113.1:p.Gly162=
|
|
XM_011526546.1:c.486G>T
|
XP_011524848.1:p.Gly162=
|
|
XM_011526547.1:c.486G>T
|
XP_011524849.1:p.Gly162=
|
|
XM_011526548.1:c.484+2460G>T
|
XP_011524850.1:n.484+2460G>T
|
|
XM_011526549.1:c.-75-31G>T
|
XP_011524851.1:n.-75-31G>T
|
|
XM_011526550.1:c.364+2460G>T
|
XP_011524852.1:n.364+2460G>T
|
|
NM_000767.5:c.486G>T
MANE Select
|
NP_000758.1:p.Gly162=
|
|