ENST00000435881.7:c.684G>T
MANE Select
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ENSP00000416627.1:p.Leu228=
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ENST00000246912.8:c.846G>T
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ENSP00000246912.3:p.Leu282=
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ENST00000346833.8:c.594G>T
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ENSP00000320913.3:p.Leu198=
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ENST00000435881.6:c.684G>T
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ENSP00000416627.1:p.Leu228=
|
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ENST00000585403.5:n.891G>T
|
|
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ENST00000588320.1:n.1160G>T
|
|
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ENST00000590050.5:n.850G>T
|
|
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NM_170607.2:c.846G>T
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NP_733752.1:p.Leu282=
|
|
NM_198204.1:c.684G>T
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NP_937847.1:p.Leu228=
|
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NM_198205.1:c.594G>T
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NP_937848.1:p.Leu198=
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|
NM_198204.2:c.684G>T
MANE Select
|
NP_937847.1:p.Leu228=
|
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NM_170607.3:c.846G>T
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NP_733752.1:p.Leu282=
|
|
NM_198205.2:c.594G>T
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NP_937848.1:p.Leu198=
|
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