ENST00000224721.12:c.6496G>C
MANE Select
|
ENSP00000224721.9:p.Asp2166His
|
|
ENST00000224721.10:c.6511G>C
|
ENSP00000224721.8:p.Asp2171His
|
|
ENST00000622827.4:c.6496G>C
|
ENSP00000483211.1:p.Asp2166His
|
|
NM_022124.5:c.6496G>C
|
NP_071407.4:p.Asp2166His
|
|
XM_006717940.2:c.6691G>C
|
XP_006718003.1:p.Asp2231His
|
|
XM_006717942.2:c.6625G>C
|
XP_006718005.1:p.Asp2209His
|
|
XM_011540039.1:c.6688G>C
|
XP_011538341.1:p.Asp2230His
|
|
XM_011540040.1:c.6685G>C
|
XP_011538342.1:p.Asp2229His
|
|
XM_011540041.1:c.6631G>C
|
XP_011538343.1:p.Asp2211His
|
|
XM_011540042.1:c.6601G>C
|
XP_011538344.1:p.Asp2201His
|
|
XM_011540043.1:c.6691G>C
|
XP_011538345.1:p.Asp2231His
|
|
XM_011540044.1:c.6556G>C
|
XP_011538346.1:p.Asp2186His
|
|
XM_011540045.1:c.6691G>C
|
XP_011538347.1:p.Asp2231His
|
|
XM_011540046.1:c.6151G>C
|
XP_011538348.1:p.Asp2051His
|
|
XM_011540047.1:c.5509G>C
|
XP_011538349.1:p.Asp1837His
|
|
XM_011540048.1:c.6691G>C
|
XP_011538350.1:p.Asp2231His
|
|
XM_011540049.1:c.6691G>C
|
XP_011538351.1:p.Asp2231His
|
|
XM_011540050.1:c.6691G>C
|
XP_011538352.1:p.Asp2231His
|
|
XM_011540051.1:c.6691G>C
|
XP_011538353.1:p.Asp2231His
|
|
XM_011540052.1:c.3019G>C
|
XP_011538354.1:p.Asp1007His
|
|
XR_945796.1:n.6934G>C
|
|
|
NM_022124.6:c.6496G>C
MANE Select
|
NP_071407.4:p.Asp2166His
|
|