ENST00000706989.1:c.2435A>G
|
ENSP00000516702.1:p.Asp812Gly
|
|
ENST00000359125.7:c.2381A>G
MANE Select
|
ENSP00000352035.2:p.Asp794Gly
|
|
ENST00000637193.1:c.1778A>G
|
ENSP00000490734.1:p.Asp593Gly
|
|
ENST00000344462.8:c.2288A>G
|
ENSP00000339611.4:p.Asp763Gly
|
|
ENST00000357249.6:c.1949A>G
|
ENSP00000349789.3:p.Asp650Gly
|
|
ENST00000359125.6:c.2381A>G
|
ENSP00000352035.2:p.Asp794Gly
|
|
ENST00000360480.7:c.2297A>G
|
ENSP00000353668.3:p.Asp766Gly
|
|
ENST00000370224.5:c.2241+164A>G
|
ENSP00000359244.2:n.2241+164A>G
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|
ENST00000625514.2:c.2205+164A>G
|
ENSP00000486040.1:n.2205+164A>G
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|
ENST00000626839.2:c.2327A>G
|
ENSP00000486706.1:p.Asp776Gly
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|
ENST00000629241.2:c.2133+164A>G
|
ENSP00000487142.1:n.2133+164A>G
|
|
ENST00000629676.2:c.1680-6039A>G
|
ENSP00000486194.1:n.1680-6039A>G
|
|
NM_004518.4:c.2297A>G
|
NP_004509.2:p.Asp766Gly
|
|
NM_172106.1:c.2327A>G
|
NP_742104.1:p.Asp776Gly
|
|
NM_172107.2:c.2381A>G
|
NP_742105.1:p.Asp794Gly
|
|
NM_172108.3:c.2288A>G
|
NP_742106.1:p.Asp763Gly
|
|
XM_006723787.1:c.2423A>G
|
XP_006723850.1:p.Asp808Gly
|
|
XM_011528807.1:c.2489A>G
|
XP_011527109.1:p.Asp830Gly
|
|
XM_011528808.1:c.2486A>G
|
XP_011527110.1:p.Asp829Gly
|
|
XM_011528809.1:c.2459A>G
|
XP_011527111.1:p.Asp820Gly
|
|
XM_011528810.1:c.2435A>G
|
XP_011527112.1:p.Asp812Gly
|
|
XM_011528811.1:c.2405A>G
|
XP_011527113.1:p.Asp802Gly
|
|
XM_011528812.1:c.2378A>G
|
XP_011527114.1:p.Asp793Gly
|
|
XM_011528813.1:c.2363A>G
|
XP_011527115.1:p.Asp788Gly
|
|
XM_011528814.1:c.1970A>G
|
XP_011527116.1:p.Asp657Gly
|
|
NM_004518.5:c.2297A>G
|
NP_004509.2:p.Asp766Gly
|
|
NM_172106.2:c.2327A>G
|
NP_742104.1:p.Asp776Gly
|
|
NM_172107.3:c.2381A>G
|
NP_742105.1:p.Asp794Gly
|
|
NM_172108.4:c.2288A>G
|
NP_742106.1:p.Asp763Gly
|
|
XM_011528810.2:c.2435A>G
|
XP_011527112.1:p.Asp812Gly
|
|
XM_011528811.2:c.2405A>G
|
XP_011527113.1:p.Asp802Gly
|
|
XM_017027841.2:c.2432A>G
|
XP_016883330.1:p.Asp811Gly
|
|
XM_017027842.2:c.2369A>G
|
XP_016883331.1:p.Asp790Gly
|
|
XM_017027843.1:c.2366A>G
|
XP_016883332.1:p.Asp789Gly
|
|
XM_017027844.2:c.2324A>G
|
XP_016883333.1:p.Asp775Gly
|
|
XM_017027845.1:c.1397A>G
|
XP_016883334.1:p.Asp466Gly
|
|
NM_004518.6:c.2297A>G
|
NP_004509.2:p.Asp766Gly
|
|
NM_172106.3:c.2327A>G
|
NP_742104.1:p.Asp776Gly
|
|
NM_172107.4:c.2381A>G
MANE Select
|
NP_742105.1:p.Asp794Gly
|
|
NM_172108.5:c.2288A>G
|
NP_742106.1:p.Asp763Gly
|
|
NM_001382235.1:c.2435A>G
|
NP_001369164.1:p.Asp812Gly
|
|