ENST00000224721.12:c.6399C>A
MANE Select
|
ENSP00000224721.9:p.Asp2133Glu
|
|
ENST00000224721.10:c.6414C>A
|
ENSP00000224721.8:p.Asp2138Glu
|
|
ENST00000622827.4:c.6399C>A
|
ENSP00000483211.1:p.Asp2133Glu
|
|
NM_022124.5:c.6399C>A
|
NP_071407.4:p.Asp2133Glu
|
|
XM_006717940.2:c.6594C>A
|
XP_006718003.1:p.Asp2198Glu
|
|
XM_006717942.2:c.6528C>A
|
XP_006718005.1:p.Asp2176Glu
|
|
XM_011540039.1:c.6591C>A
|
XP_011538341.1:p.Asp2197Glu
|
|
XM_011540040.1:c.6588C>A
|
XP_011538342.1:p.Asp2196Glu
|
|
XM_011540041.1:c.6534C>A
|
XP_011538343.1:p.Asp2178Glu
|
|
XM_011540042.1:c.6577+17C>A
|
XP_011538344.1:n.6577+17C>A
|
|
XM_011540043.1:c.6594C>A
|
XP_011538345.1:p.Asp2198Glu
|
|
XM_011540044.1:c.6459C>A
|
XP_011538346.1:p.Asp2153Glu
|
|
XM_011540045.1:c.6594C>A
|
XP_011538347.1:p.Asp2198Glu
|
|
XM_011540046.1:c.6054C>A
|
XP_011538348.1:p.Asp2018Glu
|
|
XM_011540047.1:c.5412C>A
|
XP_011538349.1:p.Asp1804Glu
|
|
XM_011540048.1:c.6594C>A
|
XP_011538350.1:p.Asp2198Glu
|
|
XM_011540049.1:c.6594C>A
|
XP_011538351.1:p.Asp2198Glu
|
|
XM_011540050.1:c.6594C>A
|
XP_011538352.1:p.Asp2198Glu
|
|
XM_011540051.1:c.6594C>A
|
XP_011538353.1:p.Asp2198Glu
|
|
XM_011540052.1:c.2922C>A
|
XP_011538354.1:p.Asp974Glu
|
|
XR_945796.1:n.6837C>A
|
|
|
NM_022124.6:c.6399C>A
MANE Select
|
NP_071407.4:p.Asp2133Glu
|
|