ENST00000288840.10:c.991_992insCAC
MANE Select
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ENSP00000288840.5:p.Trp331delinsSerArg
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ENST00000288840.9:c.991_992insCAC
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ENSP00000288840.5:p.Trp331delinsSerArg
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ENST00000557916.5:c.1123_1124insCAC
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ENSP00000452955.1:n.1123_1124insCAC
|
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ENST00000559931.5:c.295_296insCAC
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ENSP00000453446.1:n.295_296insCAC
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NM_005585.4:c.991_992insCAC
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NP_005576.3:p.Trp331delinsSerArg
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NR_027654.1:n.2046_2047insCAC
|
|
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XM_011521561.1:c.208_209insCAC
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XP_011519863.1:p.Trp70delinsSerArg
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XR_931825.1:n.2390_2391insCAC
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|
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XM_011521561.2:c.208_209insCAC
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XP_011519863.1:p.Trp70delinsSerArg
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NM_005585.5:c.991_992insCAC
MANE Select
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NP_005576.3:p.Trp331delinsSerArg
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NR_027654.2:n.2146_2147insCAC
|
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