ENST00000598742.6:c.293G>T
MANE Select
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ENSP00000470972.1:p.Ser98Ile
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ENST00000600467.6:c.293G>T
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ENSP00000469228.2:p.Ser98Ile
|
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ENST00000221975.6:c.71G>T
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ENSP00000221975.2:p.Ser24Ile
|
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ENST00000593863.5:c.293G>T
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ENSP00000470004.1:p.Ser98Ile
|
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ENST00000598399.1:c.1131G>T
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ENSP00000472660.1:n.1131G>T
|
|
ENST00000598742.5:c.293G>T
|
ENSP00000470972.1:p.Ser98Ile
|
|
NM_001022.3:c.293G>T
|
NP_001013.1:p.Ser98Ile
|
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NM_001321483.1:c.293G>T
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NP_001308412.1:p.Ser98Ile
|
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NM_001321484.1:c.293G>T
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NP_001308413.1:p.Ser98Ile
|
|
NM_001321485.1:c.306G>T
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NP_001308414.1:p.Glu102Asp
|
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XM_017027113.2:c.293G>T
|
XP_016882602.1:p.Ser98Ile
|
|
NM_001022.4:c.293G>T
MANE Select
|
NP_001013.1:p.Ser98Ile
|
|
NM_001321483.2:c.293G>T
|
NP_001308412.1:p.Ser98Ile
|
|
NM_001321484.2:c.293G>T
|
NP_001308413.1:p.Ser98Ile
|
|
NM_001321485.2:c.306G>T
|
NP_001308414.1:p.Glu102Asp
|
|