ENST00000706989.1:c.2491A>C
|
ENSP00000516702.1:p.Asn831His
|
|
ENST00000359125.7:c.2437A>C
MANE Select
|
ENSP00000352035.2:p.Asn813His
|
|
ENST00000637193.1:c.1834A>C
|
ENSP00000490734.1:p.Asn612His
|
|
ENST00000344462.8:c.2344A>C
|
ENSP00000339611.4:p.Asn782His
|
|
ENST00000357249.6:c.2005A>C
|
ENSP00000349789.3:p.Asn669His
|
|
ENST00000359125.6:c.2437A>C
|
ENSP00000352035.2:p.Asn813His
|
|
ENST00000360480.7:c.2353A>C
|
ENSP00000353668.3:p.Asn785His
|
|
ENST00000370224.5:c.2241+220A>C
|
ENSP00000359244.2:n.2241+220A>C
|
|
ENST00000625514.2:c.2205+220A>C
|
ENSP00000486040.1:n.2205+220A>C
|
|
ENST00000626839.2:c.2383A>C
|
ENSP00000486706.1:p.Asn795His
|
|
ENST00000629241.2:c.2133+220A>C
|
ENSP00000487142.1:n.2133+220A>C
|
|
ENST00000629676.2:c.1680-5983A>C
|
ENSP00000486194.1:n.1680-5983A>C
|
|
NM_004518.4:c.2353A>C
|
NP_004509.2:p.Asn785His
|
|
NM_172106.1:c.2383A>C
|
NP_742104.1:p.Asn795His
|
|
NM_172107.2:c.2437A>C
|
NP_742105.1:p.Asn813His
|
|
NM_172108.3:c.2344A>C
|
NP_742106.1:p.Asn782His
|
|
XM_006723787.1:c.2479A>C
|
XP_006723850.1:p.Asn827His
|
|
XM_011528807.1:c.2545A>C
|
XP_011527109.1:p.Asn849His
|
|
XM_011528808.1:c.2542A>C
|
XP_011527110.1:p.Asn848His
|
|
XM_011528809.1:c.2515A>C
|
XP_011527111.1:p.Asn839His
|
|
XM_011528810.1:c.2491A>C
|
XP_011527112.1:p.Asn831His
|
|
XM_011528811.1:c.2461A>C
|
XP_011527113.1:p.Asn821His
|
|
XM_011528812.1:c.2434A>C
|
XP_011527114.1:p.Asn812His
|
|
XM_011528813.1:c.2419A>C
|
XP_011527115.1:p.Asn807His
|
|
XM_011528814.1:c.2026A>C
|
XP_011527116.1:p.Asn676His
|
|
NM_004518.5:c.2353A>C
|
NP_004509.2:p.Asn785His
|
|
NM_172106.2:c.2383A>C
|
NP_742104.1:p.Asn795His
|
|
NM_172107.3:c.2437A>C
|
NP_742105.1:p.Asn813His
|
|
NM_172108.4:c.2344A>C
|
NP_742106.1:p.Asn782His
|
|
XM_011528810.2:c.2491A>C
|
XP_011527112.1:p.Asn831His
|
|
XM_011528811.2:c.2461A>C
|
XP_011527113.1:p.Asn821His
|
|
XM_017027841.2:c.2488A>C
|
XP_016883330.1:p.Asn830His
|
|
XM_017027842.2:c.2425A>C
|
XP_016883331.1:p.Asn809His
|
|
XM_017027843.1:c.2422A>C
|
XP_016883332.1:p.Asn808His
|
|
XM_017027844.2:c.2380A>C
|
XP_016883333.1:p.Asn794His
|
|
XM_017027845.1:c.1453A>C
|
XP_016883334.1:p.Asn485His
|
|
NM_004518.6:c.2353A>C
|
NP_004509.2:p.Asn785His
|
|
NM_172106.3:c.2383A>C
|
NP_742104.1:p.Asn795His
|
|
NM_172107.4:c.2437A>C
MANE Select
|
NP_742105.1:p.Asn813His
|
|
NM_172108.5:c.2344A>C
|
NP_742106.1:p.Asn782His
|
|
NM_001382235.1:c.2491A>C
|
NP_001369164.1:p.Asn831His
|
|