ENST00000369689.6:c.299T>G
MANE Select
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ENSP00000358703.1:p.Leu100Arg
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ENST00000369687.2:c.125T>G
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ENSP00000358701.1:p.Leu42Arg
|
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ENST00000369689.5:c.299T>G
|
ENSP00000358703.1:p.Leu100Arg
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ENST00000635617.1:n.3712T>G
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|
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NM_001009994.2:c.299T>G
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NP_001009994.1:p.Leu100Arg
|
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NR_103525.1:n.356T>G
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|
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NR_103525.2:n.294T>G
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|
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NM_001009994.3:c.299T>G
MANE Select
|
NP_001009994.1:p.Leu100Arg
|
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NM_001400774.1:c.-28+3140T>G
|
NP_001387703.1:n.-28+3140T>G
|
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NM_001400899.1:c.362T>G
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NP_001387828.1:p.Leu121Arg
|
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NM_001400900.1:c.*3136T>G
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NP_001387829.1:n.*3136T>G
|
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NR_174603.1:n.234+3140T>G
|
|
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NR_174604.1:n.296+3140T>G
|
|
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NR_174605.1:n.455+3242T>G
|
|
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NR_174622.1:n.3374T>G
|
|
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