ENST00000320005.6:c.2313_2316delinsAAGG
MANE Select
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ENSP00000316605.5:p.Arg771=
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ENST00000681546.1:n.2133_2136delinsAAGG
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ENST00000681746.1:c.*724_*727delinsAAGG
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ENSP00000505959.1:n.*724_*727delinsAAGG
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ENST00000320005.5:c.2313_2316delinsAAGG
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ENSP00000316605.5:p.Arg771=
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ENST00000517327.5:c.276+2768_276+2771delinsAAGG
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ENSP00000428329.1:n.276+2768_276+2771delinsAAGG
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NM_019098.4:c.2313_2316delinsAAGG
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NP_061971.3:p.Arg771=
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XM_011517138.1:c.1899_1902delinsAAGG
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XP_011515440.1:p.Arg633=
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XM_011517138.2:c.1899_1902delinsAAGG
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XP_011515440.1:p.Arg633=
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NM_019098.5:c.2313_2316delinsAAGG
MANE Select
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NP_061971.3:p.Arg771=
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