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ENST00000647165.2:c.6353T=
MANE Select
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ENSP00000495481.1:p.Leu2118=
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ENST00000205890.9:c.6353T=
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ENSP00000205890.5:p.Leu2118=
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ENST00000615845.4:c.6353T=
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ENSP00000481642.1:p.Leu2118=
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NM_016239.3:c.6353T=
|
NP_057323.3:p.Leu2118=
|
|
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XM_011523917.1:c.6293T=
|
XP_011522219.1:p.Leu2098=
|
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XM_011523918.1:c.6293T=
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XP_011522220.1:p.Leu2098=
|
|
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XM_011523921.1:c.6347T=
|
XP_011522223.1:p.Leu2116=
|
|
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XR_934037.1:n.6952T=
|
|
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XR_934038.1:n.6952T=
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|
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XM_011523918.2:c.6293T=
|
XP_011522220.1:p.Leu2098=
|
|
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XM_017024714.2:c.6293T=
|
XP_016880203.1:p.Leu2098=
|
|
|
XM_017024715.2:c.6356T=
|
XP_016880204.1:p.Leu2119=
|
|
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XM_024450781.1:c.6213+1359T=
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XP_024306549.1:n.6213+1359T=
|
|
|
NM_016239.4:c.6353T=
MANE Select
|
NP_057323.3:p.Leu2118=
|
|
