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ENSP00000418014.2:p.Arg1729=
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ENST00000636633.2:n.2194-68T>C
|
|
|
ENST00000636999.2:n.562T>C
|
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|
ENST00000288139.11:c.5187T>C
MANE Plus Clinical
|
ENSP00000288139.3:p.Arg1729=
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ENST00000350061.11:c.5127T>C
MANE Select
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ENSP00000288133.5:p.Arg1709=
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ENST00000422281.7:c.5082T>C
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ENSP00000409174.2:p.Arg1694=
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ENST00000636448.1:c.1316-68T>C
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ENST00000636570.1:c.5082T>C
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ENSP00000490183.1:p.Arg1694=
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ENST00000636629.1:n.483T>C
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ENST00000636633.1:n.2194-68T>C
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|
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ENST00000636999.1:n.554T>C
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|
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ENST00000637424.1:c.5154T>C
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ENSP00000489769.1:p.Arg1718=
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ENST00000288139.8:c.5187T>C
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ENSP00000288139.3:p.Arg1729=
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|
ENST00000350061.9:c.5127T>C
|
ENSP00000288133.5:p.Arg1709=
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|
ENST00000422281.6:c.5082T>C
|
ENSP00000409174.2:p.Arg1694=
|
|
ENST00000481478.1:c.4206T>C
|
ENSP00000418014.1:p.Arg1402=
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NM_000720.3:c.5187T>C
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NP_000711.1:p.Arg1729=
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|
NM_001128839.2:c.5082T>C
|
NP_001122311.1:p.Arg1694=
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|
NM_001128840.2:c.5127T>C
|
NP_001122312.1:p.Arg1709=
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|
XM_005265448.2:c.5082T>C
|
XP_005265505.1:p.Arg1694=
|
|
XM_011534094.1:c.5382T>C
|
XP_011532396.1:p.Arg1794=
|
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XM_011534095.1:c.5271T>C
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XP_011532397.1:p.Arg1757=
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XM_011534096.1:c.5193T>C
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XP_011532398.1:p.Arg1731=
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XM_011534097.1:c.4845T>C
|
XP_011532399.1:p.Arg1615=
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XM_011534098.1:c.4845T>C
|
XP_011532400.1:p.Arg1615=
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XM_011534099.1:c.4470T>C
|
XP_011532401.1:p.Arg1490=
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|
XM_011534100.1:c.5277T>C
|
XP_011532402.1:p.Arg1759=
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XM_005265448.3:c.5082T>C
|
XP_005265505.1:p.Arg1694=
|
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XM_011534094.2:c.5382T>C
|
XP_011532396.1:p.Arg1794=
|
|
XM_011534096.2:c.5193T>C
|
XP_011532398.1:p.Arg1731=
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XM_011534097.2:c.4845T>C
|
XP_011532399.1:p.Arg1615=
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XM_011534099.2:c.4470T>C
|
XP_011532401.1:p.Arg1490=
|
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XM_011534100.2:c.5277T>C
|
XP_011532402.1:p.Arg1759=
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XM_017007137.1:c.5382T>C
|
XP_016862626.1:p.Arg1794=
|
|
XM_017007138.1:c.5379T>C
|
XP_016862627.1:p.Arg1793=
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|
XM_017007139.1:c.5382T>C
|
XP_016862628.1:p.Arg1794=
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XM_017007140.1:c.5322T>C
|
XP_016862629.1:p.Arg1774=
|
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XM_017007141.1:c.5322T>C
|
XP_016862630.1:p.Arg1774=
|
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XM_017007142.1:c.5298T>C
|
XP_016862631.1:p.Arg1766=
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XM_017007143.1:c.5298T>C
|
XP_016862632.1:p.Arg1766=
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XM_017007144.1:c.5298T>C
|
XP_016862633.1:p.Arg1766=
|
|
XM_017007145.1:c.5253T>C
|
XP_016862634.1:p.Arg1751=
|
|
NM_001128840.3:c.5127T>C
MANE Select
|
NP_001122312.1:p.Arg1709=
|
|
NM_000720.4:c.5187T>C
MANE Plus Clinical
|
NP_000711.1:p.Arg1729=
|
|
NM_001128839.3:c.5082T>C
|
NP_001122311.1:p.Arg1694=
|
|