ENST00000350026.11:c.3088A>C
|
ENSP00000055163.8:p.Arg1030=
|
|
ENST00000414678.8:c.2998A>C
|
ENSP00000412835.3:p.Arg1000=
|
|
ENST00000637015.2:c.3088A>C
|
ENSP00000489729.2:p.Arg1030=
|
|
ENST00000319584.11:c.1102A>C
|
ENSP00000313006.7:p.Arg368=
|
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ENST00000346085.10:c.3127A>C
|
ENSP00000344546.5:p.Arg1043=
|
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ENST00000350026.10:c.2839A>C
|
ENSP00000055163.7:p.Arg947=
|
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ENST00000414678.7:c.1246A>C
|
ENSP00000412835.2:p.Arg416=
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ENST00000452544.2:n.989A>C
|
|
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ENST00000635849.1:c.409A>C
|
ENSP00000490948.1:p.Arg137=
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|
ENST00000635957.1:c.43A>C
|
ENSP00000490385.1:p.Arg15=
|
|
ENST00000636426.1:n.222A>C
|
|
|
ENST00000636930.2:c.3088A>C
MANE Select
|
ENSP00000490491.2:p.Arg1030=
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|
ENST00000637015.1:c.327A>C
|
|
|
ENST00000637568.1:c.131A>C
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ENST00000637810.1:c.589A>C
|
ENSP00000489636.1:p.Arg197=
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|
ENST00000637904.1:c.589A>C
|
ENSP00000490550.1:p.Arg197=
|
|
ENST00000647938.1:c.2878A>C
|
ENSP00000498155.1:p.Arg960=
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ENST00000674190.1:n.1837A>C
|
|
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ENST00000319584.10:c.1105A>C
|
ENSP00000313006.6:p.Arg369=
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ENST00000346085.9:c.2878A>C
|
ENSP00000344546.4:p.Arg960=
|
|
ENST00000350026.9:c.2839A>C
|
ENSP00000055163.7:p.Arg947=
|
|
ENST00000400790.3:c.40A>C
|
ENSP00000383596.3:p.Arg14=
|
|
ENST00000414678.6:c.1246A>C
|
ENSP00000412835.2:p.Arg416=
|
|
ENST00000452544.1:n.935A>C
|
|
|
ENST00000478761.3:c.161A>C
|
|
|
NM_017519.2:c.2839A>C
|
NP_059989.2:p.Arg947=
|
|
NM_020732.3:c.2878A>C
|
NP_065783.3:p.Arg960=
|
|
XM_005267069.3:c.2839A>C
|
XP_005267126.2:p.Arg947=
|
|
XM_011535984.1:c.1789A>C
|
XP_011534286.1:p.Arg597=
|
|
XM_011535985.1:c.1609A>C
|
XP_011534287.1:p.Arg537=
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|
XM_011535986.1:c.1369A>C
|
XP_011534288.1:p.Arg457=
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|
XM_011535987.1:c.988A>C
|
XP_011534289.1:p.Arg330=
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XM_011535988.1:c.-20+15743A>C
|
XP_011534290.1:n.-20+15743A>C
|
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NM_001346813.1:c.2839A>C
|
NP_001333742.1:p.Arg947=
|
|
NM_001363725.1:c.589A>C
|
NP_001350654.1:p.Arg197=
|
|
XM_011535984.2:c.2920A>C
|
XP_011534286.2:p.Arg974=
|
|
XM_011535988.3:c.-20+15743A>C
|
XP_011534290.1:n.-20+15743A>C
|
|
XM_017011103.2:c.2920A>C
|
XP_016866592.1:p.Arg974=
|
|
XM_017011104.1:c.2920A>C
|
XP_016866593.1:p.Arg974=
|
|
XM_017011105.2:c.2920A>C
|
XP_016866594.1:p.Arg974=
|
|
XM_017011106.2:c.2920A>C
|
XP_016866595.1:p.Arg974=
|
|
XM_017011107.2:c.2740A>C
|
XP_016866596.1:p.Arg914=
|
|
XR_002956289.1:n.3003A>C
|
|
|
NM_001363725.2:c.589A>C
|
NP_001350654.1:p.Arg197=
|
|
NM_001371656.1:c.3127A>C
|
NP_001358585.1:p.Arg1043=
|
|
NM_001374820.1:c.3127A>C
|
NP_001361749.1:p.Arg1043=
|
|
NM_001374828.1:c.3088A>C
MANE Select
|
NP_001361757.1:p.Arg1030=
|
|
NM_017519.3:c.3088A>C
|
NP_059989.3:p.Arg1030=
|
|