ENST00000350026.11:c.4779G=
|
ENSP00000055163.8:p.Met1593=
|
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ENST00000414678.8:c.4848G=
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ENSP00000412835.3:p.Met1616=
|
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ENST00000637015.2:c.5067G=
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ENSP00000489729.2:p.Met1689=
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ENST00000346085.10:c.4818G=
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ENSP00000344546.5:p.Met1606=
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ENST00000350026.10:c.4530G=
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ENSP00000055163.7:p.Met1510=
|
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ENST00000414678.7:c.3096G=
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ENSP00000412835.2:p.Met1032=
|
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ENST00000635849.1:c.2259G=
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ENSP00000490948.1:p.Met753=
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ENST00000635957.1:c.1890G=
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ENSP00000490385.1:p.Met630=
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ENST00000636227.1:n.3401G=
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ENST00000636254.1:n.858G=
|
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ENST00000636930.2:c.4938G=
MANE Select
|
ENSP00000490491.2:p.Met1646=
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ENST00000636940.1:n.2935G=
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ENST00000637015.1:c.2306G=
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ENST00000637568.1:c.2220G=
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ENST00000637741.1:n.1604G=
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ENST00000637810.1:c.2280G=
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ENSP00000489636.1:p.Met760=
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ENST00000637904.1:c.2439G=
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ENSP00000490550.1:p.Met813=
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ENST00000647938.1:c.4569G=
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ENSP00000498155.1:p.Met1523=
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ENST00000346085.9:c.4569G=
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ENSP00000344546.4:p.Met1523=
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ENST00000350026.9:c.4530G=
|
ENSP00000055163.7:p.Met1510=
|
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ENST00000414678.6:c.3096G=
|
ENSP00000412835.2:p.Met1032=
|
|
NM_017519.2:c.4530G=
|
NP_059989.2:p.Met1510=
|
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NM_020732.3:c.4569G=
|
NP_065783.3:p.Met1523=
|
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XM_005267069.3:c.4689G=
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XP_005267126.2:p.Met1563=
|
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XM_011535984.1:c.3768G=
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XP_011534286.1:p.Met1256=
|
|
XM_011535985.1:c.3588G=
|
XP_011534287.1:p.Met1196=
|
|
XM_011535986.1:c.3348G=
|
XP_011534288.1:p.Met1116=
|
|
XM_011535987.1:c.2967G=
|
XP_011534289.1:p.Met989=
|
|
XM_011535988.1:c.1830G=
|
XP_011534290.1:p.Met610=
|
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NM_001346813.1:c.4689G=
|
NP_001333742.1:p.Met1563=
|
|
NM_001363725.1:c.2439G=
|
NP_001350654.1:p.Met813=
|
|
XM_011535984.2:c.4899G=
|
XP_011534286.2:p.Met1633=
|
|
XM_011535988.3:c.1830G=
|
XP_011534290.1:p.Met610=
|
|
XM_017011103.2:c.4800G=
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XP_016866592.1:p.Met1600=
|
|
XM_017011104.1:c.4770G=
|
XP_016866593.1:p.Met1590=
|
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XM_017011105.2:c.4740G=
|
XP_016866594.1:p.Met1580=
|
|
XM_017011106.2:c.4611G=
|
XP_016866595.1:p.Met1537=
|
|
XM_017011107.2:c.4590G=
|
XP_016866596.1:p.Met1530=
|
|
XR_002956289.1:n.4885G=
|
|
|
NM_001363725.2:c.2439G=
|
NP_001350654.1:p.Met813=
|
|
NM_001371656.1:c.4818G=
|
NP_001358585.1:p.Met1606=
|
|
NM_001374820.1:c.4818G=
|
NP_001361749.1:p.Met1606=
|
|
NM_001374828.1:c.4938G=
MANE Select
|
NP_001361757.1:p.Met1646=
|
|
NM_017519.3:c.4779G=
|
NP_059989.3:p.Met1593=
|
|