ENST00000304611.13:c.1322T=
MANE Select
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ENSP00000303511.8:p.Leu441=
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ENST00000244546.4:c.1322T=
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ENSP00000244546.4:p.Leu441=
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|
ENST00000304611.12:c.1322T=
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ENSP00000303511.8:p.Leu441=
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NM_000287.3:c.1322T=
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NP_000278.3:p.Leu441=
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|
NM_001316313.1:c.1058T=
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NP_001303242.1:p.Leu353=
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|
NR_133009.1:n.1415T=
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|
|
XM_011514661.1:c.1238T=
|
XP_011512963.1:p.Leu413=
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|
XR_926246.1:n.1415T=
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|
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XM_011514661.2:c.1238T=
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XP_011512963.1:p.Leu413=
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|
XR_001743466.2:n.2396T=
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|
|
NM_000287.4:c.1322T=
MANE Select
|
NP_000278.3:p.Leu441=
|
|
NM_001316313.2:c.1058T=
|
NP_001303242.1:p.Leu353=
|
|
NR_133009.2:n.1353T=
|
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