ENST00000264613.11:c.2920A=
MANE Select
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ENSP00000264613.6:p.Met974=
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ENST00000264613.10:c.2920A=
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ENSP00000264613.6:p.Met974=
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ENST00000460674.5:n.837A=
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ENST00000463556.5:n.442A=
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ENST00000479771.5:c.325A=
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ENSP00000420367.1:p.Met109=
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ENST00000481169.5:c.2707A=
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ENSP00000418773.1:p.Met903=
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ENST00000490639.5:n.2952A=
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ENST00000494544.1:c.2269A=
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ENSP00000420545.1:p.Met757=
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NM_000096.3:c.2920A=
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NP_000087.1:p.Met974=
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NR_046371.1:n.2960A=
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XM_006713499.2:c.2920A=
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XP_006713562.1:p.Met974=
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XM_006713500.2:c.2920A=
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XP_006713563.1:p.Met974=
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XM_006713501.2:c.2920A=
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XP_006713564.1:p.Met974=
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XM_011512435.1:c.2920A=
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XP_011510737.1:p.Met974=
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XR_427361.2:n.3178A=
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XM_006713499.3:c.2920A=
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XP_006713562.1:p.Met974=
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XM_006713500.4:c.2920A=
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XP_006713563.1:p.Met974=
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XM_006713501.3:c.2920A=
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XP_006713564.1:p.Met974=
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XM_011512435.2:c.2920A=
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XP_011510737.1:p.Met974=
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XM_017005734.2:c.2920A=
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XP_016861223.1:p.Met974=
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XM_017005735.2:c.2920A=
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XP_016861224.1:p.Met974=
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XR_427361.3:n.3136A=
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NM_000096.4:c.2920A=
MANE Select
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NP_000087.2:p.Met974=
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NR_046371.2:n.2744A=
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