ENST00000316549.11:c.534-13699T=
MANE Select
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ENSP00000320246.6:n.534-13699T=
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ENST00000316549.10:c.534-13699T=
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ENSP00000320246.6:n.534-13699T=
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ENST00000474727.2:c.*145-13699T=
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ENSP00000419090.2:n.*145-13699T=
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NM_173653.3:c.534-13699T=
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NP_775924.1:n.534-13699T=
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XM_011512704.1:c.534-13699T=
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XP_011511006.1:n.534-13699T=
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XM_011512704.3:c.534-13699T=
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XP_011511006.1:n.534-13699T=
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XM_017006202.2:c.534-13699T=
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XP_016861691.1:n.534-13699T=
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XM_017006203.1:c.183-13699T=
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XP_016861692.1:n.183-13699T=
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NM_173653.4:c.534-13699T=
MANE Select
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NP_775924.1:n.534-13699T=
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