ENST00000706989.1:c.2497G>A
|
ENSP00000516702.1:p.Asp833Asn
|
|
ENST00000359125.7:c.2443G>A
MANE Select
|
ENSP00000352035.2:p.Asp815Asn
|
|
ENST00000637193.1:c.1840G>A
|
ENSP00000490734.1:p.Asp614Asn
|
|
ENST00000344462.8:c.2350G>A
|
ENSP00000339611.4:p.Asp784Asn
|
|
ENST00000357249.6:c.2011G>A
|
ENSP00000349789.3:p.Asp671Asn
|
|
ENST00000359125.6:c.2443G>A
|
ENSP00000352035.2:p.Asp815Asn
|
|
ENST00000360480.7:c.2359G>A
|
ENSP00000353668.3:p.Asp787Asn
|
|
ENST00000370224.5:c.2241+226G>A
|
ENSP00000359244.2:n.2241+226G>A
|
|
ENST00000625514.2:c.2205+226G>A
|
ENSP00000486040.1:n.2205+226G>A
|
|
ENST00000626839.2:c.2389G>A
|
ENSP00000486706.1:p.Asp797Asn
|
|
ENST00000629241.2:c.2133+226G>A
|
ENSP00000487142.1:n.2133+226G>A
|
|
ENST00000629676.2:c.1680-5977G>A
|
ENSP00000486194.1:n.1680-5977G>A
|
|
NM_004518.4:c.2359G>A
|
NP_004509.2:p.Asp787Asn
|
|
NM_172106.1:c.2389G>A
|
NP_742104.1:p.Asp797Asn
|
|
NM_172107.2:c.2443G>A
|
NP_742105.1:p.Asp815Asn
|
|
NM_172108.3:c.2350G>A
|
NP_742106.1:p.Asp784Asn
|
|
XM_006723787.1:c.2485G>A
|
XP_006723850.1:p.Asp829Asn
|
|
XM_011528807.1:c.2551G>A
|
XP_011527109.1:p.Asp851Asn
|
|
XM_011528808.1:c.2548G>A
|
XP_011527110.1:p.Asp850Asn
|
|
XM_011528809.1:c.2521G>A
|
XP_011527111.1:p.Asp841Asn
|
|
XM_011528810.1:c.2497G>A
|
XP_011527112.1:p.Asp833Asn
|
|
XM_011528811.1:c.2467G>A
|
XP_011527113.1:p.Asp823Asn
|
|
XM_011528812.1:c.2440G>A
|
XP_011527114.1:p.Asp814Asn
|
|
XM_011528813.1:c.2425G>A
|
XP_011527115.1:p.Asp809Asn
|
|
XM_011528814.1:c.2032G>A
|
XP_011527116.1:p.Asp678Asn
|
|
NM_004518.5:c.2359G>A
|
NP_004509.2:p.Asp787Asn
|
|
NM_172106.2:c.2389G>A
|
NP_742104.1:p.Asp797Asn
|
|
NM_172107.3:c.2443G>A
|
NP_742105.1:p.Asp815Asn
|
|
NM_172108.4:c.2350G>A
|
NP_742106.1:p.Asp784Asn
|
|
XM_011528810.2:c.2497G>A
|
XP_011527112.1:p.Asp833Asn
|
|
XM_011528811.2:c.2467G>A
|
XP_011527113.1:p.Asp823Asn
|
|
XM_017027841.2:c.2494G>A
|
XP_016883330.1:p.Asp832Asn
|
|
XM_017027842.2:c.2431G>A
|
XP_016883331.1:p.Asp811Asn
|
|
XM_017027843.1:c.2428G>A
|
XP_016883332.1:p.Asp810Asn
|
|
XM_017027844.2:c.2386G>A
|
XP_016883333.1:p.Asp796Asn
|
|
XM_017027845.1:c.1459G>A
|
XP_016883334.1:p.Asp487Asn
|
|
NM_004518.6:c.2359G>A
|
NP_004509.2:p.Asp787Asn
|
|
NM_172106.3:c.2389G>A
|
NP_742104.1:p.Asp797Asn
|
|
NM_172107.4:c.2443G>A
MANE Select
|
NP_742105.1:p.Asp815Asn
|
|
NM_172108.5:c.2350G>A
|
NP_742106.1:p.Asp784Asn
|
|
NM_001382235.1:c.2497G>A
|
NP_001369164.1:p.Asp833Asn
|
|