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|
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ENST00000642610.2:c.1125C=
MANE Select
|
ENSP00000494796.1:p.Pro375=
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|
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|
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|
|
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|
|
|
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|
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|
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|
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|
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|
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|
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|
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|
|
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|
|
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|
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|
|
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|
|
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|
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|
|
|
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|
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|
|
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|
|
|
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|
|
|
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|
|
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|
|
|
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|
|
|
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|
|
|
|
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|
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|
|
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|
|
|
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|
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|
|
|
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|
ENSP00000355560.3:p.Pro375=
|
|
|
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|
ENSP00000384571.1:p.Pro375=
|
|
|
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|
|
|
|
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|
ENSP00000439170.1:p.Pro426=
|
|
|
NM_001079515.2:c.1125C=
|
NP_001072983.1:p.Pro375=
|
|
|
NM_001287801.1:c.1278C=
|
NP_001274730.1:p.Pro426=
|
|
|
NM_001287802.1:c.786C=
|
NP_001274731.1:p.Pro262=
|
|
|
NM_003193.4:c.1125C=
|
NP_003184.1:p.Pro375=
|
|
|
NM_003193.5:c.1125C=
MANE Select
|
NP_003184.1:p.Pro375=
|
|
|
NM_001079515.3:c.1125C=
|
NP_001072983.1:p.Pro375=
|
|
|
NM_001287801.2:c.1278C=
|
NP_001274730.1:p.Pro426=
|
|
|
NM_001287802.2:c.786C=
|
NP_001274731.1:p.Pro262=
|
|
