ENST00000247138.11:c.1158G>T
MANE Select
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ENSP00000247138.5:p.Leu386=
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ENST00000247138.10:c.1158G>T
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ENSP00000247138.5:p.Leu386=
|
|
ENST00000376515.8:c.496G>T
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ENSP00000365698.3:p.Ala166Ser
|
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ENST00000376521.6:c.1158G>T
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ENSP00000365704.1:p.Leu386=
|
|
ENST00000376529.8:c.568G>T
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ENSP00000365712.3:p.Ala190Ser
|
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ENST00000413561.7:c.720G>T
|
|
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ENST00000445167.7:c.568G>T
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ENSP00000402726.2:p.Ala190Ser
|
|
ENST00000452555.7:c.1242G>T
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ENSP00000416002.2:p.Leu414=
|
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ENST00000616181.5:c.1197G>T
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ENSP00000478617.1:p.Leu399=
|
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ENST00000635285.1:c.1158G>T
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ENSP00000489484.1:p.Leu386=
|
|
ENST00000635460.1:c.425-1286G>T
|
|
|
ENST00000635589.1:c.975G>T
|
ENSP00000489197.1:p.Leu325=
|
|
ENST00000635628.1:c.*1052G>T
|
ENSP00000489613.1:n.*1052G>T
|
|
NM_001032289.2:c.568G>T
|
NP_001027460.1:p.Ala190Ser
|
|
NM_001042498.2:c.1158G>T
|
NP_001035963.1:p.Leu386=
|
|
NM_001282647.1:c.568G>T
|
NP_001269576.1:p.Ala190Ser
|
|
NM_001282648.1:c.496G>T
|
NP_001269577.1:p.Ala166Ser
|
|
NM_001282649.1:c.975G>T
|
NP_001269578.1:p.Leu325=
|
|
NM_001282650.1:c.1197G>T
|
NP_001269579.1:p.Leu399=
|
|
NM_001282651.1:c.1242G>T
|
NP_001269580.1:p.Leu414=
|
|
NM_005660.2:c.1158G>T
|
NP_005651.1:p.Leu386=
|
|
NM_005660.3:c.1158G>T
MANE Select
|
NP_005651.1:p.Leu386=
|
|
NM_001032289.3:c.568G>T
|
NP_001027460.1:p.Ala190Ser
|
|
NM_001042498.3:c.1158G>T
|
NP_001035963.1:p.Leu386=
|
|
NM_001282647.2:c.568G>T
|
NP_001269576.1:p.Ala190Ser
|
|
NM_001282649.2:c.975G>T
|
NP_001269578.1:p.Leu325=
|
|
NM_001282650.2:c.1197G>T
|
NP_001269579.1:p.Leu399=
|
|
NM_001282651.2:c.1242G>T
|
NP_001269580.1:p.Leu414=
|
|
NM_001282648.2:c.496G>T
|
NP_001269577.1:p.Ala166Ser
|
|