ENST00000350026.11:c.3972G=
|
ENSP00000055163.8:p.Met1324=
|
|
ENST00000414678.8:c.4041G=
|
ENSP00000412835.3:p.Met1347=
|
|
ENST00000637015.2:c.4260G=
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ENSP00000489729.2:p.Met1420=
|
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ENST00000346085.10:c.4011G=
|
ENSP00000344546.5:p.Met1337=
|
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ENST00000350026.10:c.3723G=
|
ENSP00000055163.7:p.Met1241=
|
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ENST00000414678.7:c.2289G=
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ENSP00000412835.2:p.Met763=
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ENST00000635849.1:c.1452G=
|
ENSP00000490948.1:p.Met484=
|
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ENST00000635957.1:c.1083G=
|
ENSP00000490385.1:p.Met361=
|
|
ENST00000636930.2:c.4131G=
MANE Select
|
ENSP00000490491.2:p.Met1377=
|
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ENST00000636940.1:n.2128G=
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|
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ENST00000637015.1:c.1499G=
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ENST00000637568.1:c.1413G=
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ENST00000637741.1:n.797G=
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ENST00000637810.1:c.1473G=
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ENSP00000489636.1:p.Met491=
|
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ENST00000637904.1:c.1632G=
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ENSP00000490550.1:p.Met544=
|
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ENST00000647938.1:c.3762G=
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ENSP00000498155.1:p.Met1254=
|
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ENST00000346085.9:c.3762G=
|
ENSP00000344546.4:p.Met1254=
|
|
ENST00000350026.9:c.3723G=
|
ENSP00000055163.7:p.Met1241=
|
|
ENST00000414678.6:c.2289G=
|
ENSP00000412835.2:p.Met763=
|
|
NM_017519.2:c.3723G=
|
NP_059989.2:p.Met1241=
|
|
NM_020732.3:c.3762G=
|
NP_065783.3:p.Met1254=
|
|
XM_005267069.3:c.3882G=
|
XP_005267126.2:p.Met1294=
|
|
XM_011535984.1:c.2961G=
|
XP_011534286.1:p.Met987=
|
|
XM_011535985.1:c.2781G=
|
XP_011534287.1:p.Met927=
|
|
XM_011535986.1:c.2541G=
|
XP_011534288.1:p.Met847=
|
|
XM_011535987.1:c.2160G=
|
XP_011534289.1:p.Met720=
|
|
XM_011535988.1:c.1023G=
|
XP_011534290.1:p.Met341=
|
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NM_001346813.1:c.3882G=
|
NP_001333742.1:p.Met1294=
|
|
NM_001363725.1:c.1632G=
|
NP_001350654.1:p.Met544=
|
|
XM_011535984.2:c.4092G=
|
XP_011534286.2:p.Met1364=
|
|
XM_011535988.3:c.1023G=
|
XP_011534290.1:p.Met341=
|
|
XM_017011103.2:c.3993G=
|
XP_016866592.1:p.Met1331=
|
|
XM_017011104.1:c.3963G=
|
XP_016866593.1:p.Met1321=
|
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XM_017011105.2:c.3933G=
|
XP_016866594.1:p.Met1311=
|
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XM_017011106.2:c.3804G=
|
XP_016866595.1:p.Met1268=
|
|
XM_017011107.2:c.3783G=
|
XP_016866596.1:p.Met1261=
|
|
XR_002956289.1:n.4175G=
|
|
|
NM_001363725.2:c.1632G=
|
NP_001350654.1:p.Met544=
|
|
NM_001371656.1:c.4011G=
|
NP_001358585.1:p.Met1337=
|
|
NM_001374820.1:c.4011G=
|
NP_001361749.1:p.Met1337=
|
|
NM_001374828.1:c.4131G=
MANE Select
|
NP_001361757.1:p.Met1377=
|
|
NM_017519.3:c.3972G=
|
NP_059989.3:p.Met1324=
|
|