ENST00000350026.11:c.4791C>T
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ENSP00000055163.8:p.Ala1597=
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ENST00000414678.8:c.4860C>T
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ENSP00000412835.3:p.Ala1620=
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ENST00000637015.2:c.5079C>T
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ENSP00000489729.2:p.Ala1693=
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ENST00000346085.10:c.4830C>T
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ENSP00000344546.5:p.Ala1610=
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ENST00000350026.10:c.4542C>T
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ENSP00000055163.7:p.Ala1514=
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ENST00000414678.7:c.3108C>T
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ENSP00000412835.2:p.Ala1036=
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ENST00000635849.1:c.2271C>T
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ENSP00000490948.1:p.Ala757=
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ENST00000635957.1:c.1902C>T
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ENSP00000490385.1:p.Ala634=
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ENST00000636227.1:n.3413C>T
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|
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ENST00000636254.1:n.870C>T
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|
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ENST00000636930.2:c.4950C>T
MANE Select
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ENSP00000490491.2:p.Ala1650=
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ENST00000636940.1:n.2947C>T
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|
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ENST00000637015.1:c.2318C>T
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|
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ENST00000637568.1:c.2232C>T
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|
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ENST00000637741.1:n.1616C>T
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|
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ENST00000637810.1:c.2292C>T
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ENSP00000489636.1:p.Ala764=
|
|
ENST00000637904.1:c.2451C>T
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ENSP00000490550.1:p.Ala817=
|
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ENST00000647938.1:c.4581C>T
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ENSP00000498155.1:p.Ala1527=
|
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ENST00000346085.9:c.4581C>T
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ENSP00000344546.4:p.Ala1527=
|
|
ENST00000350026.9:c.4542C>T
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ENSP00000055163.7:p.Ala1514=
|
|
ENST00000414678.6:c.3108C>T
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ENSP00000412835.2:p.Ala1036=
|
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NM_017519.2:c.4542C>T
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NP_059989.2:p.Ala1514=
|
|
NM_020732.3:c.4581C>T
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NP_065783.3:p.Ala1527=
|
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XM_005267069.3:c.4701C>T
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XP_005267126.2:p.Ala1567=
|
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XM_011535984.1:c.3780C>T
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XP_011534286.1:p.Ala1260=
|
|
XM_011535985.1:c.3600C>T
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XP_011534287.1:p.Ala1200=
|
|
XM_011535986.1:c.3360C>T
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XP_011534288.1:p.Ala1120=
|
|
XM_011535987.1:c.2979C>T
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XP_011534289.1:p.Ala993=
|
|
XM_011535988.1:c.1842C>T
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XP_011534290.1:p.Ala614=
|
|
NM_001346813.1:c.4701C>T
|
NP_001333742.1:p.Ala1567=
|
|
NM_001363725.1:c.2451C>T
|
NP_001350654.1:p.Ala817=
|
|
XM_011535984.2:c.4911C>T
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XP_011534286.2:p.Ala1637=
|
|
XM_011535988.3:c.1842C>T
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XP_011534290.1:p.Ala614=
|
|
XM_017011103.2:c.4812C>T
|
XP_016866592.1:p.Ala1604=
|
|
XM_017011104.1:c.4782C>T
|
XP_016866593.1:p.Ala1594=
|
|
XM_017011105.2:c.4752C>T
|
XP_016866594.1:p.Ala1584=
|
|
XM_017011106.2:c.4623C>T
|
XP_016866595.1:p.Ala1541=
|
|
XM_017011107.2:c.4602C>T
|
XP_016866596.1:p.Ala1534=
|
|
XR_002956289.1:n.4897C>T
|
|
|
NM_001363725.2:c.2451C>T
|
NP_001350654.1:p.Ala817=
|
|
NM_001371656.1:c.4830C>T
|
NP_001358585.1:p.Ala1610=
|
|
NM_001374820.1:c.4830C>T
|
NP_001361749.1:p.Ala1610=
|
|
NM_001374828.1:c.4950C>T
MANE Select
|
NP_001361757.1:p.Ala1650=
|
|
NM_017519.3:c.4791C>T
|
NP_059989.3:p.Ala1597=
|
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