ENST00000234071.8:c.1153A=
MANE Select
|
ENSP00000234071.4:p.Met385=
|
|
ENST00000234071.7:c.1153A=
|
ENSP00000234071.3:p.Met385=
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|
ENST00000402125.2:c.477A=
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|
|
ENST00000409048.1:c.1255A=
|
ENSP00000386679.1:p.Met419=
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|
NM_000312.3:c.1153A= , LRG_599t1:c.1153A=
|
NP_000303.1:p.Met385=
|
|
XM_005263715.3:c.1336A=
|
XP_005263772.1:p.Met446=
|
|
XM_005263716.3:c.1318A=
|
XP_005263773.1:p.Met440=
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|
XM_005263717.3:c.1216A=
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XP_005263774.1:p.Met406=
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|
XR_923313.1:n.1332-449T=
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|
|
XM_005263717.4:c.1216A=
|
XP_005263774.1:p.Met406=
|
|
XM_017004505.1:c.1396A=
|
XP_016859994.1:p.Met466=
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|
XM_024453002.1:c.1498A=
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XP_024308770.1:p.Met500=
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|
XM_024453003.1:c.1438A=
|
XP_024308771.1:p.Met480=
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|
XM_024453004.1:c.1336A=
|
XP_024308772.1:p.Met446=
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|
XM_024453005.1:c.1318A=
|
XP_024308773.1:p.Met440=
|
|
XM_024453006.1:c.1255A=
|
XP_024308774.1:p.Met419=
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|
XR_001739705.1:n.3607-449T=
|
|
|
XR_923313.2:n.4043-449T=
|
|
|
NM_000312.4:c.1153A=
MANE Select
|
NP_000303.1:p.Met385=
|
|
NM_001375602.1:c.1336A=
|
NP_001362531.1:p.Met446=
|
|
NM_001375603.1:c.1318A=
|
NP_001362532.1:p.Met440=
|
|
NM_001375604.1:c.1216A=
|
NP_001362533.1:p.Met406=
|
|
NM_001375605.1:c.1255A=
|
NP_001362534.1:p.Met419=
|
|
NM_001375606.1:c.1321A=
|
NP_001362535.1:p.Met441=
|
|
NM_001375607.1:c.1339A=
|
NP_001362536.1:p.Met447=
|
|
NM_001375608.1:c.1096A=
|
NP_001362537.1:p.Met366=
|
|
NM_001375609.1:c.1129A=
|
NP_001362538.1:p.Met377=
|
|
NM_001375610.1:c.1147A=
|
NP_001362539.1:p.Met383=
|
|
NM_001375611.1:c.1153A=
|
NP_001362540.1:p.Met385=
|
|
NM_001375613.1:c.1153A=
|
NP_001362542.1:p.Met385=
|
|