ENST00000455537.7:c.2933G>T
MANE Select
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ENSP00000408979.2:p.Ser978Ile
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ENST00000674619.1:c.2954G>T
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ENSP00000502270.1:p.Ser985Ile
|
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ENST00000675697.1:c.24G>T
|
|
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ENST00000675737.1:n.337G>T
|
|
|
ENST00000675882.1:n.2456G>T
|
|
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ENST00000675929.1:n.1491G>T
|
|
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ENST00000676055.1:c.24G>T
|
|
|
ENST00000676457.1:c.2828G>T
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ENSP00000501588.1:p.Ser943Ile
|
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ENST00000286452.5:c.2666G>T
|
ENSP00000286452.5:p.Ser889Ile
|
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ENST00000455537.6:c.2933G>T
|
ENSP00000408979.2:p.Ser978Ile
|
|
ENST00000552227.1:n.216G>T
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|
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NM_004984.2:c.2933G>T
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NP_004975.2:p.Ser978Ile
|
|
NM_001354705.1:c.2666G>T
|
NP_001341634.1:p.Ser889Ile
|
|
NM_004984.3:c.2933G>T
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NP_004975.2:p.Ser978Ile
|
|
XR_002957324.1:n.3166G>T
|
|
|
NM_004984.4:c.2933G>T
MANE Select
|
NP_004975.2:p.Ser978Ile
|
|
NM_001354705.2:c.2666G>T
|
NP_001341634.1:p.Ser889Ile
|
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