ENST00000224721.12:c.4507G>C
MANE Select
|
ENSP00000224721.9:p.Gly1503Arg
|
|
ENST00000224721.10:c.4522G>C
|
ENSP00000224721.8:p.Gly1508Arg
|
|
ENST00000398792.3:n.1196G>C
|
|
|
ENST00000622827.4:c.4507G>C
|
ENSP00000483211.1:p.Gly1503Arg
|
|
NM_022124.5:c.4507G>C
|
NP_071407.4:p.Gly1503Arg
|
|
XM_006717940.2:c.4702G>C
|
XP_006718003.1:p.Gly1568Arg
|
|
XM_006717942.2:c.4636G>C
|
XP_006718005.1:p.Gly1546Arg
|
|
XM_011540039.1:c.4699G>C
|
XP_011538341.1:p.Gly1567Arg
|
|
XM_011540040.1:c.4696G>C
|
XP_011538342.1:p.Gly1566Arg
|
|
XM_011540041.1:c.4642G>C
|
XP_011538343.1:p.Gly1548Arg
|
|
XM_011540042.1:c.4702G>C
|
XP_011538344.1:p.Gly1568Arg
|
|
XM_011540043.1:c.4702G>C
|
XP_011538345.1:p.Gly1568Arg
|
|
XM_011540044.1:c.4567G>C
|
XP_011538346.1:p.Gly1523Arg
|
|
XM_011540045.1:c.4702G>C
|
XP_011538347.1:p.Gly1568Arg
|
|
XM_011540046.1:c.4162G>C
|
XP_011538348.1:p.Gly1388Arg
|
|
XM_011540047.1:c.3520G>C
|
XP_011538349.1:p.Gly1174Arg
|
|
XM_011540048.1:c.4702G>C
|
XP_011538350.1:p.Gly1568Arg
|
|
XM_011540049.1:c.4702G>C
|
XP_011538351.1:p.Gly1568Arg
|
|
XM_011540050.1:c.4702G>C
|
XP_011538352.1:p.Gly1568Arg
|
|
XM_011540051.1:c.4702G>C
|
XP_011538353.1:p.Gly1568Arg
|
|
XM_011540052.1:c.1030G>C
|
XP_011538354.1:p.Gly344Arg
|
|
XM_011540053.1:c.4702G>C
|
XP_011538355.1:p.Gly1568Arg
|
|
XR_945796.1:n.4945G>C
|
|
|
NM_022124.6:c.4507G>C
MANE Select
|
NP_071407.4:p.Gly1503Arg
|
|