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ENST00000510025.7:c.522T=
MANE Select
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NM_000414.3:c.522T=
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NM_001292028.1:c.102T=
|
NP_001278957.1:p.Leu34=
|
|
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NM_000414.4:c.522T=
MANE Select
|
NP_000405.1:p.Leu174=
|
|
|
NM_001199291.3:c.597T=
|
NP_001186220.1:p.Leu199=
|
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NM_001199292.2:c.468T=
|
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|
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|
NM_001292027.2:c.450T=
|
NP_001278956.1:p.Leu150=
|
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NM_001292028.2:c.102T=
|
NP_001278957.1:p.Leu34=
|
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NM_001374497.1:c.513T=
|
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|
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|
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|
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NM_001374499.1:c.195T=
|
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|
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|
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|
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NM_001374501.1:c.111T=
|
NP_001361430.1:p.Leu37=
|
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NM_001374502.1:c.111T=
|
NP_001361431.1:p.Leu37=
|
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|
NM_001374503.1:c.111T=
|
NP_001361432.1:p.Leu37=
|
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NR_164653.1:n.601T=
|
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NR_164654.1:n.789T=
|
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