ENST00000350026.11:c.4671G>T
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ENSP00000055163.8:p.Ala1557=
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ENST00000414678.8:c.4740G>T
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ENSP00000412835.3:p.Ala1580=
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ENST00000637015.2:c.4959G>T
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ENSP00000489729.2:p.Ala1653=
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ENST00000346085.10:c.4710G>T
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ENSP00000344546.5:p.Ala1570=
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ENST00000350026.10:c.4422G>T
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ENSP00000055163.7:p.Ala1474=
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ENST00000414678.7:c.2988G>T
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ENSP00000412835.2:p.Ala996=
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ENST00000635849.1:c.2151G>T
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ENSP00000490948.1:p.Ala717=
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ENST00000635957.1:c.1782G>T
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ENSP00000490385.1:p.Ala594=
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ENST00000636227.1:n.3293G>T
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|
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ENST00000636254.1:n.750G>T
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ENST00000636930.2:c.4830G>T
MANE Select
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ENSP00000490491.2:p.Ala1610=
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ENST00000636940.1:n.2827G>T
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|
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ENST00000637015.1:c.2198G>T
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|
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ENST00000637568.1:c.2112G>T
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|
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ENST00000637741.1:n.1496G>T
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|
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ENST00000637810.1:c.2172G>T
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ENSP00000489636.1:p.Ala724=
|
|
ENST00000637904.1:c.2331G>T
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ENSP00000490550.1:p.Ala777=
|
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ENST00000647938.1:c.4461G>T
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ENSP00000498155.1:p.Ala1487=
|
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ENST00000346085.9:c.4461G>T
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ENSP00000344546.4:p.Ala1487=
|
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ENST00000350026.9:c.4422G>T
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ENSP00000055163.7:p.Ala1474=
|
|
ENST00000414678.6:c.2988G>T
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ENSP00000412835.2:p.Ala996=
|
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NM_017519.2:c.4422G>T
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NP_059989.2:p.Ala1474=
|
|
NM_020732.3:c.4461G>T
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NP_065783.3:p.Ala1487=
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XM_005267069.3:c.4581G>T
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XP_005267126.2:p.Ala1527=
|
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XM_011535984.1:c.3660G>T
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XP_011534286.1:p.Ala1220=
|
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XM_011535985.1:c.3480G>T
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XP_011534287.1:p.Ala1160=
|
|
XM_011535986.1:c.3240G>T
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XP_011534288.1:p.Ala1080=
|
|
XM_011535987.1:c.2859G>T
|
XP_011534289.1:p.Ala953=
|
|
XM_011535988.1:c.1722G>T
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XP_011534290.1:p.Ala574=
|
|
NM_001346813.1:c.4581G>T
|
NP_001333742.1:p.Ala1527=
|
|
NM_001363725.1:c.2331G>T
|
NP_001350654.1:p.Ala777=
|
|
XM_011535984.2:c.4791G>T
|
XP_011534286.2:p.Ala1597=
|
|
XM_011535988.3:c.1722G>T
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XP_011534290.1:p.Ala574=
|
|
XM_017011103.2:c.4692G>T
|
XP_016866592.1:p.Ala1564=
|
|
XM_017011104.1:c.4662G>T
|
XP_016866593.1:p.Ala1554=
|
|
XM_017011105.2:c.4632G>T
|
XP_016866594.1:p.Ala1544=
|
|
XM_017011106.2:c.4503G>T
|
XP_016866595.1:p.Ala1501=
|
|
XM_017011107.2:c.4482G>T
|
XP_016866596.1:p.Ala1494=
|
|
XR_002956289.1:n.4777G>T
|
|
|
NM_001363725.2:c.2331G>T
|
NP_001350654.1:p.Ala777=
|
|
NM_001371656.1:c.4710G>T
|
NP_001358585.1:p.Ala1570=
|
|
NM_001374820.1:c.4710G>T
|
NP_001361749.1:p.Ala1570=
|
|
NM_001374828.1:c.4830G>T
MANE Select
|
NP_001361757.1:p.Ala1610=
|
|
NM_017519.3:c.4671G>T
|
NP_059989.3:p.Ala1557=
|
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