ENST00000302068.9:c.1170G>A
MANE Select
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ENSP00000306099.4:p.Leu390=
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ENST00000302068.8:c.1170G>A
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ENSP00000306099.4:p.Leu390=
|
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ENST00000502545.5:n.939+418G>A
|
|
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ENST00000509493.1:c.513G>A
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ENSP00000426757.1:p.Leu171=
|
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NM_001184741.1:c.993G>A
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NP_001171670.1:p.Leu331=
|
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NM_005141.4:c.1170G>A , LRG_558t1:c.1170G>A
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NP_005132.2:p.Leu390=
|
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NM_001382759.1:c.1038G>A
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NP_001369688.1:p.Leu346=
|
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NM_001382760.1:c.1170G>A
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NP_001369689.1:p.Leu390=
|
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NM_001382761.1:c.1170G>A
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NP_001369690.1:p.Leu390=
|
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NM_001382762.1:c.870G>A
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NP_001369691.1:p.Leu290=
|
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NM_001382763.1:c.1161G>A
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NP_001369692.1:p.Leu387=
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NM_001382764.1:c.1081-48G>A
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NP_001369693.1:n.1081-48G>A
|
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NM_001382765.1:c.1170G>A
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NP_001369694.1:p.Leu390=
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|
NM_005141.5:c.1170G>A
MANE Select
|
NP_005132.2:p.Leu390=
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