ENST00000350026.11:c.3448A=
|
ENSP00000055163.8:p.Met1150=
|
|
ENST00000414678.8:c.3517A=
|
ENSP00000412835.3:p.Met1173=
|
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ENST00000637015.2:c.3736A=
|
ENSP00000489729.2:p.Met1246=
|
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ENST00000319584.11:c.1621A=
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ENSP00000313006.7:p.Met541=
|
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ENST00000346085.10:c.3487A=
|
ENSP00000344546.5:p.Met1163=
|
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ENST00000350026.10:c.3199A=
|
ENSP00000055163.7:p.Met1067=
|
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ENST00000414678.7:c.1765A=
|
ENSP00000412835.2:p.Met589=
|
|
ENST00000635849.1:c.928A=
|
ENSP00000490948.1:p.Met310=
|
|
ENST00000635957.1:c.562A=
|
ENSP00000490385.1:p.Met188=
|
|
ENST00000636930.2:c.3607A=
MANE Select
|
ENSP00000490491.2:p.Met1203=
|
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ENST00000636940.1:n.1604A=
|
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ENST00000637015.1:c.975A=
|
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ENST00000637568.1:c.889A=
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ENST00000637741.1:n.273A=
|
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ENST00000637810.1:c.949A=
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ENSP00000489636.1:p.Met317=
|
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ENST00000637904.1:c.1108A=
|
ENSP00000490550.1:p.Met370=
|
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ENST00000647938.1:c.3238A=
|
ENSP00000498155.1:p.Met1080=
|
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ENST00000319584.10:c.1624A=
|
ENSP00000313006.6:p.Met542=
|
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ENST00000346085.9:c.3238A=
|
ENSP00000344546.4:p.Met1080=
|
|
ENST00000350026.9:c.3199A=
|
ENSP00000055163.7:p.Met1067=
|
|
ENST00000400790.3:c.400A=
|
ENSP00000383596.3:p.Met134=
|
|
ENST00000414678.6:c.1765A=
|
ENSP00000412835.2:p.Met589=
|
|
ENST00000478761.3:c.809A=
|
|
|
NM_017519.2:c.3199A=
|
NP_059989.2:p.Met1067=
|
|
NM_020732.3:c.3238A=
|
NP_065783.3:p.Met1080=
|
|
XM_005267069.3:c.3358A=
|
XP_005267126.2:p.Met1120=
|
|
XM_011535984.1:c.2437A=
|
XP_011534286.1:p.Met813=
|
|
XM_011535985.1:c.2257A=
|
XP_011534287.1:p.Met753=
|
|
XM_011535986.1:c.2017A=
|
XP_011534288.1:p.Met673=
|
|
XM_011535987.1:c.1636A=
|
XP_011534289.1:p.Met546=
|
|
XM_011535988.1:c.499A=
|
XP_011534290.1:p.Met167=
|
|
NM_001346813.1:c.3358A=
|
NP_001333742.1:p.Met1120=
|
|
NM_001363725.1:c.1108A=
|
NP_001350654.1:p.Met370=
|
|
XM_011535984.2:c.3568A=
|
XP_011534286.2:p.Met1190=
|
|
XM_011535988.3:c.499A=
|
XP_011534290.1:p.Met167=
|
|
XM_017011103.2:c.3469A=
|
XP_016866592.1:p.Met1157=
|
|
XM_017011104.1:c.3439A=
|
XP_016866593.1:p.Met1147=
|
|
XM_017011105.2:c.3409A=
|
XP_016866594.1:p.Met1137=
|
|
XM_017011106.2:c.3280A=
|
XP_016866595.1:p.Met1094=
|
|
XM_017011107.2:c.3259A=
|
XP_016866596.1:p.Met1087=
|
|
XR_002956289.1:n.3651A=
|
|
|
NM_001363725.2:c.1108A=
|
NP_001350654.1:p.Met370=
|
|
NM_001371656.1:c.3487A=
|
NP_001358585.1:p.Met1163=
|
|
NM_001374820.1:c.3487A=
|
NP_001361749.1:p.Met1163=
|
|
NM_001374828.1:c.3607A=
MANE Select
|
NP_001361757.1:p.Met1203=
|
|
NM_017519.3:c.3448A=
|
NP_059989.3:p.Met1150=
|
|