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ENST00000642610.2:c.1254C=
MANE Select
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ENSP00000494796.1:p.Tyr418=
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ENST00000642764.1:n.2085C=
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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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ENST00000647322.1:c.845C=
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|
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|
ENST00000651186.1:c.915C=
|
ENSP00000498645.1:p.Tyr305=
|
|
|
ENST00000366601.7:c.1254C=
|
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|
|
|
ENST00000406207.4:c.1254C=
|
ENSP00000384571.1:p.Tyr418=
|
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|
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|
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|
ENST00000543662.3:c.1407C=
|
ENSP00000439170.1:p.Tyr469=
|
|
|
NM_001079515.2:c.1254C=
|
NP_001072983.1:p.Tyr418=
|
|
|
NM_001287801.1:c.1407C=
|
NP_001274730.1:p.Tyr469=
|
|
|
NM_001287802.1:c.915C=
|
NP_001274731.1:p.Tyr305=
|
|
|
NM_003193.4:c.1254C=
|
NP_003184.1:p.Tyr418=
|
|
|
NM_003193.5:c.1254C=
MANE Select
|
NP_003184.1:p.Tyr418=
|
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|
NM_001079515.3:c.1254C=
|
NP_001072983.1:p.Tyr418=
|
|
|
NM_001287801.2:c.1407C=
|
NP_001274730.1:p.Tyr469=
|
|
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NM_001287802.2:c.915C=
|
NP_001274731.1:p.Tyr305=
|
|
