ENST00000224721.12:c.4555G>C
MANE Select
|
ENSP00000224721.9:p.Asp1519His
|
|
ENST00000224721.10:c.4570G>C
|
ENSP00000224721.8:p.Asp1524His
|
|
ENST00000398792.3:n.1244G>C
|
|
|
ENST00000622827.4:c.4555G>C
|
ENSP00000483211.1:p.Asp1519His
|
|
NM_022124.5:c.4555G>C
|
NP_071407.4:p.Asp1519His
|
|
XM_006717940.2:c.4750G>C
|
XP_006718003.1:p.Asp1584His
|
|
XM_006717942.2:c.4684G>C
|
XP_006718005.1:p.Asp1562His
|
|
XM_011540039.1:c.4747G>C
|
XP_011538341.1:p.Asp1583His
|
|
XM_011540040.1:c.4744G>C
|
XP_011538342.1:p.Asp1582His
|
|
XM_011540041.1:c.4690G>C
|
XP_011538343.1:p.Asp1564His
|
|
XM_011540042.1:c.4750G>C
|
XP_011538344.1:p.Asp1584His
|
|
XM_011540043.1:c.4750G>C
|
XP_011538345.1:p.Asp1584His
|
|
XM_011540044.1:c.4615G>C
|
XP_011538346.1:p.Asp1539His
|
|
XM_011540045.1:c.4750G>C
|
XP_011538347.1:p.Asp1584His
|
|
XM_011540046.1:c.4210G>C
|
XP_011538348.1:p.Asp1404His
|
|
XM_011540047.1:c.3568G>C
|
XP_011538349.1:p.Asp1190His
|
|
XM_011540048.1:c.4750G>C
|
XP_011538350.1:p.Asp1584His
|
|
XM_011540049.1:c.4750G>C
|
XP_011538351.1:p.Asp1584His
|
|
XM_011540050.1:c.4750G>C
|
XP_011538352.1:p.Asp1584His
|
|
XM_011540051.1:c.4750G>C
|
XP_011538353.1:p.Asp1584His
|
|
XM_011540052.1:c.1078G>C
|
XP_011538354.1:p.Asp360His
|
|
XM_011540053.1:c.4750G>C
|
XP_011538355.1:p.Asp1584His
|
|
XR_945796.1:n.4993G>C
|
|
|
NM_022124.6:c.4555G>C
MANE Select
|
NP_071407.4:p.Asp1519His
|
|