ENST00000706989.1:c.2641G>C
|
ENSP00000516702.1:p.Gly881Arg
|
|
ENST00000359125.7:c.2587G>C
MANE Select
|
ENSP00000352035.2:p.Gly863Arg
|
|
ENST00000637193.1:c.1984G>C
|
ENSP00000490734.1:p.Gly662Arg
|
|
ENST00000344462.8:c.2494G>C
|
ENSP00000339611.4:p.Gly832Arg
|
|
ENST00000357249.6:c.2155G>C
|
ENSP00000349789.3:p.Gly719Arg
|
|
ENST00000359125.6:c.2587G>C
|
ENSP00000352035.2:p.Gly863Arg
|
|
ENST00000360480.7:c.2503G>C
|
ENSP00000353668.3:p.Gly835Arg
|
|
ENST00000370224.5:c.2241+370G>C
|
ENSP00000359244.2:n.2241+370G>C
|
|
ENST00000625514.2:c.2205+370G>C
|
ENSP00000486040.1:n.2205+370G>C
|
|
ENST00000626839.2:c.2533G>C
|
ENSP00000486706.1:p.Gly845Arg
|
|
ENST00000629241.2:c.2133+370G>C
|
ENSP00000487142.1:n.2133+370G>C
|
|
ENST00000629676.2:c.1680-5833G>C
|
ENSP00000486194.1:n.1680-5833G>C
|
|
NM_004518.4:c.2503G>C
|
NP_004509.2:p.Gly835Arg
|
|
NM_172106.1:c.2533G>C
|
NP_742104.1:p.Gly845Arg
|
|
NM_172107.2:c.2587G>C
|
NP_742105.1:p.Gly863Arg
|
|
NM_172108.3:c.2494G>C
|
NP_742106.1:p.Gly832Arg
|
|
XM_006723787.1:c.2629G>C
|
XP_006723850.1:p.Gly877Arg
|
|
XM_011528807.1:c.2695G>C
|
XP_011527109.1:p.Gly899Arg
|
|
XM_011528808.1:c.2692G>C
|
XP_011527110.1:p.Gly898Arg
|
|
XM_011528809.1:c.2665G>C
|
XP_011527111.1:p.Gly889Arg
|
|
XM_011528810.1:c.2641G>C
|
XP_011527112.1:p.Gly881Arg
|
|
XM_011528811.1:c.2611G>C
|
XP_011527113.1:p.Gly871Arg
|
|
XM_011528812.1:c.2584G>C
|
XP_011527114.1:p.Gly862Arg
|
|
XM_011528813.1:c.2569G>C
|
XP_011527115.1:p.Gly857Arg
|
|
XM_011528814.1:c.2176G>C
|
XP_011527116.1:p.Gly726Arg
|
|
NM_004518.5:c.2503G>C
|
NP_004509.2:p.Gly835Arg
|
|
NM_172106.2:c.2533G>C
|
NP_742104.1:p.Gly845Arg
|
|
NM_172107.3:c.2587G>C
|
NP_742105.1:p.Gly863Arg
|
|
NM_172108.4:c.2494G>C
|
NP_742106.1:p.Gly832Arg
|
|
XM_011528810.2:c.2641G>C
|
XP_011527112.1:p.Gly881Arg
|
|
XM_011528811.2:c.2611G>C
|
XP_011527113.1:p.Gly871Arg
|
|
XM_017027841.2:c.2638G>C
|
XP_016883330.1:p.Gly880Arg
|
|
XM_017027842.2:c.2575G>C
|
XP_016883331.1:p.Gly859Arg
|
|
XM_017027843.1:c.2572G>C
|
XP_016883332.1:p.Gly858Arg
|
|
XM_017027844.2:c.2530G>C
|
XP_016883333.1:p.Gly844Arg
|
|
XM_017027845.1:c.1603G>C
|
XP_016883334.1:p.Gly535Arg
|
|
NM_004518.6:c.2503G>C
|
NP_004509.2:p.Gly835Arg
|
|
NM_172106.3:c.2533G>C
|
NP_742104.1:p.Gly845Arg
|
|
NM_172107.4:c.2587G>C
MANE Select
|
NP_742105.1:p.Gly863Arg
|
|
NM_172108.5:c.2494G>C
|
NP_742106.1:p.Gly832Arg
|
|
NM_001382235.1:c.2641G>C
|
NP_001369164.1:p.Gly881Arg
|
|