ENST00000224721.12:c.6402A>C
MANE Select
|
ENSP00000224721.9:p.Arg2134Ser
|
|
ENST00000224721.10:c.6417A>C
|
ENSP00000224721.8:p.Arg2139Ser
|
|
ENST00000622827.4:c.6402A>C
|
ENSP00000483211.1:p.Arg2134Ser
|
|
NM_022124.5:c.6402A>C
|
NP_071407.4:p.Arg2134Ser
|
|
XM_006717940.2:c.6597A>C
|
XP_006718003.1:p.Arg2199Ser
|
|
XM_006717942.2:c.6531A>C
|
XP_006718005.1:p.Arg2177Ser
|
|
XM_011540039.1:c.6594A>C
|
XP_011538341.1:p.Arg2198Ser
|
|
XM_011540040.1:c.6591A>C
|
XP_011538342.1:p.Arg2197Ser
|
|
XM_011540041.1:c.6537A>C
|
XP_011538343.1:p.Arg2179Ser
|
|
XM_011540042.1:c.6577+20A>C
|
XP_011538344.1:n.6577+20A>C
|
|
XM_011540043.1:c.6597A>C
|
XP_011538345.1:p.Arg2199Ser
|
|
XM_011540044.1:c.6462A>C
|
XP_011538346.1:p.Arg2154Ser
|
|
XM_011540045.1:c.6597A>C
|
XP_011538347.1:p.Arg2199Ser
|
|
XM_011540046.1:c.6057A>C
|
XP_011538348.1:p.Arg2019Ser
|
|
XM_011540047.1:c.5415A>C
|
XP_011538349.1:p.Arg1805Ser
|
|
XM_011540048.1:c.6597A>C
|
XP_011538350.1:p.Arg2199Ser
|
|
XM_011540049.1:c.6597A>C
|
XP_011538351.1:p.Arg2199Ser
|
|
XM_011540050.1:c.6597A>C
|
XP_011538352.1:p.Arg2199Ser
|
|
XM_011540051.1:c.6597A>C
|
XP_011538353.1:p.Arg2199Ser
|
|
XM_011540052.1:c.2925A>C
|
XP_011538354.1:p.Arg975Ser
|
|
XR_945796.1:n.6840A>C
|
|
|
NM_022124.6:c.6402A>C
MANE Select
|
NP_071407.4:p.Arg2134Ser
|
|