ENST00000288840.10:c.997_999delinsAGC
MANE Select
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ENSP00000288840.5:p.Ser333=
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ENST00000288840.9:c.997_999delinsAGC
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ENSP00000288840.5:p.Ser333=
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ENST00000557916.5:c.1129_1131delinsAGC
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ENSP00000452955.1:n.1129_1131delinsAGC
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ENST00000559931.5:c.301_303delinsAGC
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ENSP00000453446.1:n.301_303delinsAGC
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NM_005585.4:c.997_999delinsAGC
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NP_005576.3:p.Ser333=
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NR_027654.1:n.2052_2054delinsAGC
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XM_011521561.1:c.214_216delinsAGC
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XP_011519863.1:p.Ser72=
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XR_931825.1:n.2396_2398delinsAGC
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XM_011521561.2:c.214_216delinsAGC
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XP_011519863.1:p.Ser72=
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|
NM_005585.5:c.997_999delinsAGC
MANE Select
|
NP_005576.3:p.Ser333=
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NR_027654.2:n.2152_2154delinsAGC
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