ENST00000224721.12:c.6414G>A
MANE Select
|
ENSP00000224721.9:p.Glu2138=
|
|
ENST00000224721.10:c.6429G>A
|
ENSP00000224721.8:p.Glu2143=
|
|
ENST00000622827.4:c.6414G>A
|
ENSP00000483211.1:p.Glu2138=
|
|
NM_022124.5:c.6414G>A
|
NP_071407.4:p.Glu2138=
|
|
XM_006717940.2:c.6609G>A
|
XP_006718003.1:p.Glu2203=
|
|
XM_006717942.2:c.6543G>A
|
XP_006718005.1:p.Glu2181=
|
|
XM_011540039.1:c.6606G>A
|
XP_011538341.1:p.Glu2202=
|
|
XM_011540040.1:c.6603G>A
|
XP_011538342.1:p.Glu2201=
|
|
XM_011540041.1:c.6549G>A
|
XP_011538343.1:p.Glu2183=
|
|
XM_011540042.1:c.6577+32G>A
|
XP_011538344.1:n.6577+32G>A
|
|
XM_011540043.1:c.6609G>A
|
XP_011538345.1:p.Glu2203=
|
|
XM_011540044.1:c.6474G>A
|
XP_011538346.1:p.Glu2158=
|
|
XM_011540045.1:c.6609G>A
|
XP_011538347.1:p.Glu2203=
|
|
XM_011540046.1:c.6069G>A
|
XP_011538348.1:p.Glu2023=
|
|
XM_011540047.1:c.5427G>A
|
XP_011538349.1:p.Glu1809=
|
|
XM_011540048.1:c.6609G>A
|
XP_011538350.1:p.Glu2203=
|
|
XM_011540049.1:c.6609G>A
|
XP_011538351.1:p.Glu2203=
|
|
XM_011540050.1:c.6609G>A
|
XP_011538352.1:p.Glu2203=
|
|
XM_011540051.1:c.6609G>A
|
XP_011538353.1:p.Glu2203=
|
|
XM_011540052.1:c.2937G>A
|
XP_011538354.1:p.Glu979=
|
|
XR_945796.1:n.6852G>A
|
|
|
NM_022124.6:c.6414G>A
MANE Select
|
NP_071407.4:p.Glu2138=
|
|