ENST00000706989.1:c.2296C>A
|
ENSP00000516702.1:p.His766Asn
|
|
ENST00000359125.7:c.2242C>A
MANE Select
|
ENSP00000352035.2:p.His748Asn
|
|
ENST00000637193.1:c.1639C>A
|
ENSP00000490734.1:p.His547Asn
|
|
ENST00000344462.8:c.2149C>A
|
ENSP00000339611.4:p.His717Asn
|
|
ENST00000357249.6:c.1810C>A
|
ENSP00000349789.3:p.His604Asn
|
|
ENST00000359125.6:c.2242C>A
|
ENSP00000352035.2:p.His748Asn
|
|
ENST00000360480.7:c.2158C>A
|
ENSP00000353668.3:p.His720Asn
|
|
ENST00000370224.5:c.2241+25C>A
|
ENSP00000359244.2:n.2241+25C>A
|
|
ENST00000625514.2:c.2205+25C>A
|
ENSP00000486040.1:n.2205+25C>A
|
|
ENST00000626839.2:c.2188C>A
|
ENSP00000486706.1:p.His730Asn
|
|
ENST00000629241.2:c.2133+25C>A
|
ENSP00000487142.1:n.2133+25C>A
|
|
ENST00000629676.2:c.1680-6178C>A
|
ENSP00000486194.1:n.1680-6178C>A
|
|
NM_004518.4:c.2158C>A
|
NP_004509.2:p.His720Asn
|
|
NM_172106.1:c.2188C>A
|
NP_742104.1:p.His730Asn
|
|
NM_172107.2:c.2242C>A
|
NP_742105.1:p.His748Asn
|
|
NM_172108.3:c.2149C>A
|
NP_742106.1:p.His717Asn
|
|
XM_006723787.1:c.2284C>A
|
XP_006723850.1:p.His762Asn
|
|
XM_011528807.1:c.2350C>A
|
XP_011527109.1:p.His784Asn
|
|
XM_011528808.1:c.2347C>A
|
XP_011527110.1:p.His783Asn
|
|
XM_011528809.1:c.2320C>A
|
XP_011527111.1:p.His774Asn
|
|
XM_011528810.1:c.2296C>A
|
XP_011527112.1:p.His766Asn
|
|
XM_011528811.1:c.2266C>A
|
XP_011527113.1:p.His756Asn
|
|
XM_011528812.1:c.2239C>A
|
XP_011527114.1:p.His747Asn
|
|
XM_011528813.1:c.2224C>A
|
XP_011527115.1:p.His742Asn
|
|
XM_011528814.1:c.1831C>A
|
XP_011527116.1:p.His611Asn
|
|
NM_004518.5:c.2158C>A
|
NP_004509.2:p.His720Asn
|
|
NM_172106.2:c.2188C>A
|
NP_742104.1:p.His730Asn
|
|
NM_172107.3:c.2242C>A
|
NP_742105.1:p.His748Asn
|
|
NM_172108.4:c.2149C>A
|
NP_742106.1:p.His717Asn
|
|
XM_011528810.2:c.2296C>A
|
XP_011527112.1:p.His766Asn
|
|
XM_011528811.2:c.2266C>A
|
XP_011527113.1:p.His756Asn
|
|
XM_017027841.2:c.2293C>A
|
XP_016883330.1:p.His765Asn
|
|
XM_017027842.2:c.2230C>A
|
XP_016883331.1:p.His744Asn
|
|
XM_017027843.1:c.2227C>A
|
XP_016883332.1:p.His743Asn
|
|
XM_017027844.2:c.2185C>A
|
XP_016883333.1:p.His729Asn
|
|
XM_017027845.1:c.1258C>A
|
XP_016883334.1:p.His420Asn
|
|
NM_004518.6:c.2158C>A
|
NP_004509.2:p.His720Asn
|
|
NM_172106.3:c.2188C>A
|
NP_742104.1:p.His730Asn
|
|
NM_172107.4:c.2242C>A
MANE Select
|
NP_742105.1:p.His748Asn
|
|
NM_172108.5:c.2149C>A
|
NP_742106.1:p.His717Asn
|
|
NM_001382235.1:c.2296C>A
|
NP_001369164.1:p.His766Asn
|
|