ENST00000325366.14:c.81G>T
MANE Select
|
ENSP00000326879.9:p.Glu27Asp
|
|
ENST00000325366.13:c.81G>T
|
ENSP00000326879.9:p.Glu27Asp
|
|
ENST00000504464.5:c.81G>T
|
ENSP00000430261.1:p.Glu27Asp
|
|
ENST00000507818.6:c.81G>T
|
ENSP00000430860.1:p.Glu27Asp
|
|
ENST00000510659.5:c.81G>T
|
ENSP00000423039.1:p.Glu27Asp
|
|
ENST00000511208.2:c.81G>T
|
ENSP00000428898.1:p.Glu27Asp
|
|
ENST00000513967.5:c.81G>T
|
ENSP00000421667.1:p.Glu27Asp
|
|
ENST00000515409.5:n.179G>T
|
|
|
ENST00000517780.1:n.179G>T
|
|
|
NM_018356.2:c.81G>T
|
NP_060826.2:p.Glu27Asp
|
|
XM_005248319.2:c.-491G>T
|
XP_005248376.1:n.-491G>T
|
|
XM_006714479.1:c.-80G>T
|
XP_006714542.1:n.-80G>T
|
|
XM_006714480.2:c.-402G>T
|
XP_006714543.1:n.-402G>T
|
|
XM_011514062.1:c.81G>T
|
XP_011512364.1:p.Glu27Asp
|
|
NR_134298.1:n.208G>T
|
|
|
XM_006714479.2:c.-80G>T
|
XP_006714542.1:n.-80G>T
|
|
XM_006714480.3:c.-402G>T
|
XP_006714543.1:n.-402G>T
|
|
XM_011514062.3:c.81G>T
|
XP_011512364.1:p.Glu27Asp
|
|
XM_017009607.1:c.81G>T
|
XP_016865096.1:p.Glu27Asp
|
|
XM_017009608.2:c.81G>T
|
XP_016865097.1:p.Glu27Asp
|
|
XM_017009609.1:c.-80G>T
|
XP_016865098.1:n.-80G>T
|
|
XM_017009610.1:c.-494G>T
|
XP_016865099.1:n.-494G>T
|
|
XM_017009611.2:c.-491G>T
|
XP_016865100.1:n.-491G>T
|
|
XM_017009612.2:c.-402G>T
|
XP_016865101.1:n.-402G>T
|
|
XM_017009613.2:c.-494G>T
|
XP_016865102.1:n.-494G>T
|
|
XM_017009614.1:c.-587G>T
|
XP_016865103.1:n.-587G>T
|
|
XM_017009615.1:c.-495G>T
|
XP_016865104.1:n.-495G>T
|
|
XM_017009616.1:c.-399G>T
|
XP_016865105.1:n.-399G>T
|
|
NM_018356.3:c.81G>T
MANE Select
|
NP_060826.2:p.Glu27Asp
|
|
NR_134298.2:n.173G>T
|
|
|