ENST00000706989.1:c.2498A>C
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ENSP00000516702.1:p.Asp833Ala
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ENST00000359125.7:c.2444A>C
MANE Select
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ENSP00000352035.2:p.Asp815Ala
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ENST00000637193.1:c.1841A>C
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ENSP00000490734.1:p.Asp614Ala
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ENST00000344462.8:c.2351A>C
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ENSP00000339611.4:p.Asp784Ala
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ENST00000357249.6:c.2012A>C
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ENSP00000349789.3:p.Asp671Ala
|
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ENST00000359125.6:c.2444A>C
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ENSP00000352035.2:p.Asp815Ala
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ENST00000360480.7:c.2360A>C
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ENSP00000353668.3:p.Asp787Ala
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ENST00000370224.5:c.2241+227A>C
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ENSP00000359244.2:n.2241+227A>C
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ENST00000625514.2:c.2205+227A>C
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ENSP00000486040.1:n.2205+227A>C
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ENST00000626839.2:c.2390A>C
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ENSP00000486706.1:p.Asp797Ala
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ENST00000629241.2:c.2133+227A>C
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ENSP00000487142.1:n.2133+227A>C
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ENST00000629676.2:c.1680-5976A>C
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ENSP00000486194.1:n.1680-5976A>C
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NM_004518.4:c.2360A>C
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NP_004509.2:p.Asp787Ala
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NM_172106.1:c.2390A>C
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NP_742104.1:p.Asp797Ala
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NM_172107.2:c.2444A>C
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NP_742105.1:p.Asp815Ala
|
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NM_172108.3:c.2351A>C
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NP_742106.1:p.Asp784Ala
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XM_006723787.1:c.2486A>C
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XP_006723850.1:p.Asp829Ala
|
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XM_011528807.1:c.2552A>C
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XP_011527109.1:p.Asp851Ala
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XM_011528808.1:c.2549A>C
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XP_011527110.1:p.Asp850Ala
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XM_011528809.1:c.2522A>C
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XP_011527111.1:p.Asp841Ala
|
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XM_011528810.1:c.2498A>C
|
XP_011527112.1:p.Asp833Ala
|
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XM_011528811.1:c.2468A>C
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XP_011527113.1:p.Asp823Ala
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XM_011528812.1:c.2441A>C
|
XP_011527114.1:p.Asp814Ala
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XM_011528813.1:c.2426A>C
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XP_011527115.1:p.Asp809Ala
|
|
XM_011528814.1:c.2033A>C
|
XP_011527116.1:p.Asp678Ala
|
|
NM_004518.5:c.2360A>C
|
NP_004509.2:p.Asp787Ala
|
|
NM_172106.2:c.2390A>C
|
NP_742104.1:p.Asp797Ala
|
|
NM_172107.3:c.2444A>C
|
NP_742105.1:p.Asp815Ala
|
|
NM_172108.4:c.2351A>C
|
NP_742106.1:p.Asp784Ala
|
|
XM_011528810.2:c.2498A>C
|
XP_011527112.1:p.Asp833Ala
|
|
XM_011528811.2:c.2468A>C
|
XP_011527113.1:p.Asp823Ala
|
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XM_017027841.2:c.2495A>C
|
XP_016883330.1:p.Asp832Ala
|
|
XM_017027842.2:c.2432A>C
|
XP_016883331.1:p.Asp811Ala
|
|
XM_017027843.1:c.2429A>C
|
XP_016883332.1:p.Asp810Ala
|
|
XM_017027844.2:c.2387A>C
|
XP_016883333.1:p.Asp796Ala
|
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XM_017027845.1:c.1460A>C
|
XP_016883334.1:p.Asp487Ala
|
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NM_004518.6:c.2360A>C
|
NP_004509.2:p.Asp787Ala
|
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NM_172106.3:c.2390A>C
|
NP_742104.1:p.Asp797Ala
|
|
NM_172107.4:c.2444A>C
MANE Select
|
NP_742105.1:p.Asp815Ala
|
|
NM_172108.5:c.2351A>C
|
NP_742106.1:p.Asp784Ala
|
|
NM_001382235.1:c.2498A>C
|
NP_001369164.1:p.Asp833Ala
|
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