ENST00000706989.1:c.2187G>T
|
ENSP00000516702.1:p.Gln729His
|
|
ENST00000359125.7:c.2133G>T
MANE Select
|
ENSP00000352035.2:p.Gln711His
|
|
ENST00000637193.1:c.1530G>T
|
ENSP00000490734.1:p.Gln510His
|
|
ENST00000344462.8:c.2040G>T
|
ENSP00000339611.4:p.Gln680His
|
|
ENST00000357249.6:c.1701G>T
|
ENSP00000349789.3:p.Gln567His
|
|
ENST00000359125.6:c.2133G>T
|
ENSP00000352035.2:p.Gln711His
|
|
ENST00000360480.7:c.2049G>T
|
ENSP00000353668.3:p.Gln683His
|
|
ENST00000370224.5:c.2157G>T
|
ENSP00000359244.2:p.Gln719His
|
|
ENST00000625514.2:c.2121G>T
|
ENSP00000486040.1:p.Gln707His
|
|
ENST00000626839.2:c.2079G>T
|
ENSP00000486706.1:p.Gln693His
|
|
ENST00000629241.2:c.2049G>T
|
ENSP00000487142.1:p.Gln683His
|
|
ENST00000629676.2:c.1680-6287G>T
|
ENSP00000486194.1:n.1680-6287G>T
|
|
NM_004518.4:c.2049G>T
|
NP_004509.2:p.Gln683His
|
|
NM_172106.1:c.2079G>T
|
NP_742104.1:p.Gln693His
|
|
NM_172107.2:c.2133G>T
|
NP_742105.1:p.Gln711His
|
|
NM_172108.3:c.2040G>T
|
NP_742106.1:p.Gln680His
|
|
XM_006723787.1:c.2175G>T
|
XP_006723850.1:p.Gln725His
|
|
XM_011528807.1:c.2241G>T
|
XP_011527109.1:p.Gln747His
|
|
XM_011528808.1:c.2238G>T
|
XP_011527110.1:p.Gln746His
|
|
XM_011528809.1:c.2211G>T
|
XP_011527111.1:p.Gln737His
|
|
XM_011528810.1:c.2187G>T
|
XP_011527112.1:p.Gln729His
|
|
XM_011528811.1:c.2157G>T
|
XP_011527113.1:p.Gln719His
|
|
XM_011528812.1:c.2130G>T
|
XP_011527114.1:p.Gln710His
|
|
XM_011528813.1:c.2115G>T
|
XP_011527115.1:p.Gln705His
|
|
XM_011528814.1:c.1722G>T
|
XP_011527116.1:p.Gln574His
|
|
NM_004518.5:c.2049G>T
|
NP_004509.2:p.Gln683His
|
|
NM_172106.2:c.2079G>T
|
NP_742104.1:p.Gln693His
|
|
NM_172107.3:c.2133G>T
|
NP_742105.1:p.Gln711His
|
|
NM_172108.4:c.2040G>T
|
NP_742106.1:p.Gln680His
|
|
XM_011528810.2:c.2187G>T
|
XP_011527112.1:p.Gln729His
|
|
XM_011528811.2:c.2157G>T
|
XP_011527113.1:p.Gln719His
|
|
XM_017027841.2:c.2184G>T
|
XP_016883330.1:p.Gln728His
|
|
XM_017027842.2:c.2121G>T
|
XP_016883331.1:p.Gln707His
|
|
XM_017027843.1:c.2118G>T
|
XP_016883332.1:p.Gln706His
|
|
XM_017027844.2:c.2076G>T
|
XP_016883333.1:p.Gln692His
|
|
XM_017027845.1:c.1149G>T
|
XP_016883334.1:p.Gln383His
|
|
NM_004518.6:c.2049G>T
|
NP_004509.2:p.Gln683His
|
|
NM_172106.3:c.2079G>T
|
NP_742104.1:p.Gln693His
|
|
NM_172107.4:c.2133G>T
MANE Select
|
NP_742105.1:p.Gln711His
|
|
NM_172108.5:c.2040G>T
|
NP_742106.1:p.Gln680His
|
|
NM_001382235.1:c.2187G>T
|
NP_001369164.1:p.Gln729His
|
|