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ENSP00000362669.3:p.Met279=
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ENST00000373573.9:c.835A=
MANE Select
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ENSP00000362674.3:p.Met279=
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ENST00000373583.6:c.757A=
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ENSP00000362685.2:p.Met253=
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|
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|
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|
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|
|
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|
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|
|
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|
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ENSP00000416489.1:n.*90A=
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|
NM_018486.2:c.835A=
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NR_051952.1:n.1035A=
|
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XM_011530986.1:c.835A=
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XP_011529288.1:p.Met279=
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XM_011530987.1:c.835A=
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XP_011529289.1:p.Met279=
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|
XM_011530988.1:c.835A=
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XP_011529290.1:p.Met279=
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XR_938402.1:n.921A=
|
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XM_011530986.3:c.835A=
|
XP_011529288.3:p.Met279=
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|
XM_017029640.2:c.757A=
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XP_016885129.2:p.Met253=
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|
XM_017029641.2:c.757A=
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XP_016885130.2:p.Met253=
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XM_017029642.1:c.676A=
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XP_016885131.1:p.Met226=
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|
XM_017029643.2:c.649A=
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XP_016885132.1:p.Met217=
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|
XM_017029644.2:c.598A=
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XP_016885133.1:p.Met200=
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XM_017029645.2:c.649A=
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XP_016885134.1:p.Met217=
|
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XM_017029646.1:c.448A=
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XP_016885135.1:p.Met150=
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XM_024452405.1:c.250A=
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XP_024308173.1:p.Met84=
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XR_001755711.2:n.921A=
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XR_002958779.1:n.921A=
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XR_002958780.1:n.921A=
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XR_002958781.1:n.921A=
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XR_002958782.1:n.897A=
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XR_002958783.1:n.897A=
|
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|
XR_938402.3:n.921A=
|
|
|
NM_018486.3:c.835A=
MANE Select
|
NP_060956.1:p.Met279=
|
|
NM_001166418.2:c.562A=
|
NP_001159890.1:p.Met188=
|
|
NR_051952.2:n.775A=
|
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