ENST00000634296.2:c.*1221A=
|
ENSP00000489512.2:n.*1221A=
|
|
ENST00000673864.2:c.*2315A=
|
ENSP00000501045.2:n.*2315A=
|
|
ENST00000674147.2:c.2950A=
|
ENSP00000500964.2:p.Met984=
|
|
ENST00000242839.10:c.3571A=
MANE Select
|
ENSP00000242839.5:p.Met1191=
|
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ENST00000344297.9:c.2950A=
|
ENSP00000342559.5:p.Met984=
|
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ENST00000400366.6:c.3238A=
|
ENSP00000383217.3:p.Met1080=
|
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ENST00000448424.7:c.3319A=
|
ENSP00000416738.3:p.Met1107=
|
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ENST00000673696.1:n.812A=
|
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ENST00000673772.1:c.3337A=
|
ENSP00000501168.1:p.Met1113=
|
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ENST00000673867.1:n.3710A=
|
|
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ENST00000673923.1:n.437A=
|
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ENST00000674147.1:c.2506A=
|
ENSP00000500964.1:p.Met836=
|
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ENST00000242839.8:c.3571A=
|
ENSP00000242839.4:p.Met1191=
|
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ENST00000344297.8:c.2950A=
|
ENSP00000342559.5:p.Met984=
|
|
ENST00000400366.5:c.3238A=
|
ENSP00000383217.3:p.Met1080=
|
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ENST00000400370.8:c.2281A=
|
ENSP00000383221.3:p.Met761=
|
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ENST00000418097.7:c.3376A=
|
ENSP00000393343.2:p.Met1126=
|
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ENST00000448424.6:c.3337A=
|
ENSP00000416738.2:p.Met1113=
|
|
ENST00000634296.1:c.1349A=
|
|
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ENST00000634308.1:c.*672A=
|
ENSP00000489234.1:n.*672A=
|
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ENST00000634620.1:n.4315A=
|
|
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ENST00000634810.1:n.2916A=
|
|
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ENST00000634844.1:c.3427A=
|
ENSP00000489398.1:p.Met1143=
|
|
NM_000053.3:c.3571A=
|
NP_000044.2:p.Met1191=
|
|
NM_001005918.2:c.2950A=
|
NP_001005918.1:p.Met984=
|
|
NM_001243182.1:c.3238A=
|
NP_001230111.1:p.Met1080=
|
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XM_005266423.2:c.3475A=
|
XP_005266480.1:p.Met1159=
|
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XM_005266424.3:c.3475A=
|
XP_005266481.1:p.Met1159=
|
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XM_005266427.2:c.3337A=
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XP_005266484.1:p.Met1113=
|
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XM_005266428.1:c.3319A=
|
XP_005266485.1:p.Met1107=
|
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XM_005266430.3:c.3571A=
|
XP_005266487.1:p.Met1191=
|
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XM_005266431.2:c.3535A=
|
XP_005266488.1:p.Met1179=
|
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XM_005266432.2:c.3085A=
|
XP_005266489.1:p.Met1029=
|
|
XM_006719837.2:c.3475A=
|
XP_006719900.1:p.Met1159=
|
|
XM_006719838.1:c.1387A=
|
XP_006719901.1:p.Met463=
|
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XM_006719839.1:c.1204A=
|
XP_006719902.1:p.Met402=
|
|
XM_011535117.1:c.3475A=
|
XP_011533419.1:p.Met1159=
|
|
XM_011535118.1:c.3436A=
|
XP_011533420.1:p.Met1146=
|
|
XM_011535119.1:c.3388A=
|
XP_011533421.1:p.Met1130=
|
|
XM_011535120.1:c.3157A=
|
XP_011533422.1:p.Met1053=
|
|
XM_011535121.1:c.3058A=
|
XP_011533423.1:p.Met1020=
|
|
XM_011535122.1:c.2239A=
|
XP_011533424.1:p.Met747=
|
|
XR_941601.1:n.3790A=
|
|
|
XR_941602.1:n.3790A=
|
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|
XR_941603.1:n.3790A=
|
|
|
XR_941604.1:n.3790A=
|
|
|
NM_001330578.1:c.3337A=
|
NP_001317507.1:p.Met1113=
|
|
NM_001330579.1:c.3319A=
|
NP_001317508.1:p.Met1107=
|
|
XM_005266424.4:c.3475A=
|
XP_005266481.1:p.Met1159=
|
|
XM_005266430.4:c.3571A=
|
XP_005266487.1:p.Met1191=
|
|
XM_005266431.4:c.3535A=
|
XP_005266488.1:p.Met1179=
|
|
XM_006719837.3:c.3475A=
|
XP_006719900.1:p.Met1159=
|
|
XM_011535117.3:c.3475A=
|
XP_011533419.1:p.Met1159=
|
|
XM_017020627.1:c.3475A=
|
XP_016876116.1:p.Met1159=
|
|
NM_000053.4:c.3571A=
MANE Select
|
NP_000044.2:p.Met1191=
|
|
NM_001005918.3:c.2950A=
|
NP_001005918.1:p.Met984=
|
|
NM_001330579.2:c.3319A=
|
NP_001317508.1:p.Met1107=
|
|
NM_001243182.2:c.3238A=
|
NP_001230111.1:p.Met1080=
|
|
NM_001330578.2:c.3337A=
|
NP_001317507.1:p.Met1113=
|
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