ENST00000553645.7:c.81G>T
MANE Select
|
ENSP00000452037.1:p.Glu27Asp
|
|
ENST00000311089.7:c.-187-3102G>T
|
ENSP00000310360.3:n.-187-3102G>T
|
|
ENST00000553645.6:c.81G>T
|
ENSP00000452037.1:p.Glu27Asp
|
|
ENST00000554113.5:c.-187-3102G>T
|
ENSP00000452368.1:n.-187-3102G>T
|
|
ENST00000554159.1:c.24G>T
|
ENSP00000451264.1:p.Glu8Asp
|
|
ENST00000554339.5:c.3+13843G>T
|
ENSP00000450744.1:n.3+13843G>T
|
|
ENST00000554871.5:c.-37G>T
|
ENSP00000451834.1:n.-37G>T
|
|
ENST00000555631.6:c.-37G>T
|
ENSP00000451547.2:n.-37G>T
|
|
ENST00000555919.7:c.-37G>T
|
ENSP00000451101.2:n.-37G>T
|
|
ENST00000559993.1:c.-406G>T
|
ENSP00000453439.1:n.-406G>T
|
|
NM_001201366.1:c.-37G>T
|
NP_001188295.1:n.-37G>T
|
|
NM_031427.3:c.81G>T
|
NP_113615.2:p.Glu27Asp
|
|
XM_011537204.1:c.-37G>T
|
XP_011535506.1:n.-37G>T
|
|
XM_017021679.2:c.-37G>T
|
XP_016877168.1:n.-37G>T
|
|
XM_024449715.1:c.-37G>T
|
XP_024305483.1:n.-37G>T
|
|
NM_031427.4:c.81G>T
MANE Select
|
NP_113615.2:p.Glu27Asp
|
|
NM_001201366.2:c.-37G>T
|
NP_001188295.1:n.-37G>T
|
|