ENST00000706989.1:c.1568G>A
|
ENSP00000516702.1:p.Arg523Lys
|
|
ENST00000359125.7:c.1622G>A
MANE Select
|
ENSP00000352035.2:p.Arg541Lys
|
|
ENST00000637193.1:c.1019G>A
|
ENSP00000490734.1:p.Arg340Lys
|
|
ENST00000344462.8:c.1529G>A
|
ENSP00000339611.4:p.Arg510Lys
|
|
ENST00000357249.6:c.1190G>A
|
ENSP00000349789.3:p.Arg397Lys
|
|
ENST00000359125.6:c.1622G>A
|
ENSP00000352035.2:p.Arg541Lys
|
|
ENST00000360480.7:c.1538G>A
|
ENSP00000353668.3:p.Arg513Lys
|
|
ENST00000370224.5:c.1538G>A
|
ENSP00000359244.2:p.Arg513Lys
|
|
ENST00000625514.2:c.1502G>A
|
ENSP00000486040.1:p.Arg501Lys
|
|
ENST00000626839.2:c.1568G>A
|
ENSP00000486706.1:p.Arg523Lys
|
|
ENST00000627221.2:c.679G>A
|
|
|
ENST00000629241.2:c.1538G>A
|
ENSP00000487142.1:p.Arg513Lys
|
|
ENST00000629318.1:c.230G>A
|
ENSP00000487384.1:p.Arg77Lys
|
|
ENST00000629676.2:c.1538G>A
|
ENSP00000486194.1:p.Arg513Lys
|
|
NM_004518.4:c.1538G>A
|
NP_004509.2:p.Arg513Lys
|
|
NM_172106.1:c.1568G>A
|
NP_742104.1:p.Arg523Lys
|
|
NM_172107.2:c.1622G>A
|
NP_742105.1:p.Arg541Lys
|
|
NM_172108.3:c.1529G>A
|
NP_742106.1:p.Arg510Lys
|
|
XM_006723787.1:c.1622G>A
|
XP_006723850.1:p.Arg541Lys
|
|
XM_011528807.1:c.1622G>A
|
XP_011527109.1:p.Arg541Lys
|
|
XM_011528808.1:c.1619G>A
|
XP_011527110.1:p.Arg540Lys
|
|
XM_011528809.1:c.1592G>A
|
XP_011527111.1:p.Arg531Lys
|
|
XM_011528810.1:c.1568G>A
|
XP_011527112.1:p.Arg523Lys
|
|
XM_011528811.1:c.1538G>A
|
XP_011527113.1:p.Arg513Lys
|
|
XM_011528812.1:c.1619G>A
|
XP_011527114.1:p.Arg540Lys
|
|
XM_011528813.1:c.1496G>A
|
XP_011527115.1:p.Arg499Lys
|
|
XM_011528814.1:c.1103G>A
|
XP_011527116.1:p.Arg368Lys
|
|
XM_011528815.1:c.1622G>A
|
XP_011527117.1:p.Arg541Lys
|
|
NM_004518.5:c.1538G>A
|
NP_004509.2:p.Arg513Lys
|
|
NM_172106.2:c.1568G>A
|
NP_742104.1:p.Arg523Lys
|
|
NM_172107.3:c.1622G>A
|
NP_742105.1:p.Arg541Lys
|
|
NM_172108.4:c.1529G>A
|
NP_742106.1:p.Arg510Lys
|
|
XM_011528810.2:c.1568G>A
|
XP_011527112.1:p.Arg523Lys
|
|
XM_011528811.2:c.1538G>A
|
XP_011527113.1:p.Arg513Lys
|
|
XM_017027841.2:c.1565G>A
|
XP_016883330.1:p.Arg522Lys
|
|
XM_017027842.2:c.1568G>A
|
XP_016883331.1:p.Arg523Lys
|
|
XM_017027843.1:c.1499G>A
|
XP_016883332.1:p.Arg500Lys
|
|
XM_017027844.2:c.1565G>A
|
XP_016883333.1:p.Arg522Lys
|
|
XM_017027845.1:c.530G>A
|
XP_016883334.1:p.Arg177Lys
|
|
NM_004518.6:c.1538G>A
|
NP_004509.2:p.Arg513Lys
|
|
NM_172106.3:c.1568G>A
|
NP_742104.1:p.Arg523Lys
|
|
NM_172107.4:c.1622G>A
MANE Select
|
NP_742105.1:p.Arg541Lys
|
|
NM_172108.5:c.1529G>A
|
NP_742106.1:p.Arg510Lys
|
|
NM_001382235.1:c.1568G>A
|
NP_001369164.1:p.Arg523Lys
|
|